High molecular weight surface proteins of non-typeable haemophilus

ABSTRACT

High molecular weight surface proteins of non-typeable Haemophilus influenzae which exhibit immunogenic properties and genes encoding the same are described. Specifically, genes coding for two immunodominant high molecular weight proteins, HMW1 and HMW2, have been cloned, expressed and sequenced, while genes coding for high molecular proteins HMW3 and HMW4 have been cloned, expressed and partially sequenced.

This application is a 35 USC 371 of PCT/US94/02550 filed Mar. 15, 1994.

FIELD OF INVENTION

This invention relates to high molecular weight proteins of non-typeable haemophilus.

BACKGROUND TO THE INVENTION

Non-typeable Haemophilus influenzae are non-encapsulated organisms that are defined by their lack of reactivity with antisera against known H. influenzae capsular antigens.

These organisms commonly inhabit the upper respiratory tract of humans and are frequently responsible for infections, such as otitis media, sinusitis, conjunctivitis, bronchitis and pneumonia. Since these organisms do not have a polysaccharide capsule, they are not controlled by the present Haemophilus influenzae type b (Hib) vaccines, which are directed towards Hib bacterial capsular polysaccharides. The non-typeable strains, however, do produce surface antigens that can elicit bactericidal antibodies. Two of the major outer membrane proteins, P2 and P6, have been identified as targets of human serum bactericidal activity. However, it has been shown that the P2 protein sequence is variable, in particular in the non-typeable Haemophilus strains. Thus, a P2-based vaccine would not protect against all strains of the organism.

There have previously been identified by Barenkamp et al (Pediatr. Infect. Dis. J., 9:333-339, 1990) a group of high-molecular-weight (HMW) proteins that appeared to be major targets of antibodies present in human convalescent sera. Examination of a series of middle ear isolates revealed the presence of one or two such proteins in most strains. However, prior to the present invention, the structures of these proteins were unknown as were pure isolates of such proteins.

SUMMARY OF INVENTION

The inventors, in an effort to further characterize the high molecular weight (HMW) Haemophilus proteins, have cloned, expressed and sequenced the genes coding for two immunodominant HMW proteins (designated HMW1 and HMW2) from a prototype non-typeable Haemophilus strain and have cloned, expressed and almost completely sequenced the genes coding for two additional immunodominant HMW proteins (designated HMW3 and HMW4) from another non-typeable Haemophilus strain.

In accordance with one aspect of the present invention, therefore, there is provided an isolated and purified gene coding for a high molecular weight protein of a non-typeable Haemophilus strain, particularly a gene coding for protein HMW1, HMW2, HMW3 or HMW4, as well as any variant or fragment of such protein which retains the immunological ability to protect against disease caused by a non-typeable Haemophilus strain. In another aspect, the invention provides a high molecular weight protein of non-typeable Haemophilus influenzae which is encoded by these genes.

BRIEF DESCRIPTION OF DRAWINGS

FIGS. 1A-1G is a DNA sequence of a gene coding for protein HMW1 (SEQ ID NO: 1);

FIGS. 2A-2B is a derived amino acid sequence of protein HMW1 (SEQ ID NO: 2);

FIGS. 3A-3G is a DNA sequence of a gene coding for protein HMW2 (SEQ ID NO: 3);

FIGS. 4A-4B is a derived amino acid sequence of HMW2 (SEQ ID NO: 4);

FIG. 5A shows restriction maps of representative recombinant phages which contained the HMW1 or HMW2 structural genes, the locations of the structural genes being indicated by the shaded bars;

FIG. 5B shows the restriction map of the T7 expression vector pT7-7;

FIGS. 6A-6L contains the DNA sequence of a gene cluster for the hmw1 gene (SEQ ID NO: 5), comprising nucleotides 351 to 4958 (ORF a) (as in FIG. 1), as well as two additional downstream genes in the 3' flanking region, comprising ORFs b, nucleotides 5114-6748 and c nucleotides 7062-9011;

FIGS. 7A-7L contains the DNA sequence of a gene cluster for the hmw2 gene (SEQ ID NO: 6), comprising nucleotides 792 to 5222 (ORF a) (as in FIG. 3), as well as two additional downstream genes in the 3' flanking region, comprising ORFs b, nucleotides 5375-7009, and c, nucleotides 7249-9198;

FIGS. 8A-8F is a partial DNA sequence of a gene coding for protein HMW3 (SEQ ID NO: 7);

FIGS. 9A-9F is a partial DNA sequence of a gene coding for protein HMW4 (SEQ ID NO: 8); and

FIGS. 10A-10L is a comparison table for the derived amino acid sequence for proteins HMW1, HMW2, HMW3 and HMW4.

GENERAL DESCRIPTION OF INVENTION

The DNA sequences of the genes coding for HMW1 and HMW2, shown in FIGS. 1 and 3 respectively, were shown to be about 80% identical, with the first 1259 base pairs of the genes being identical. The derived amino acid sequences of the two HMW proteins, shown in FIGS. 2 and 4 respectively, are about 70% identical. Furthermore, the encoded proteins are antigenically related to the filamentous hemagglutinin surface protein of Bordetella pertussis. A monoclonal antibody prepared against filamentous hemagglutinin (FHA) of Bordetella pertussis was found to recognize both of the high molecular weight proteins. This data suggests that the HMW and FHA proteins may serve similar biological functions. The derived amino acid sequences of the HMW1 and HMW2 proteins show sequence similarity to that for the FHA protein. It has further been shown that these antigenically-related proteins are produced by the majority of the non-typeable strains of Haemophilus. Antisera raised against the protein expressed by the HMW1 gene recognizes both the HMW2 protein and the B. pertussis FHA. The present invention includes an isolated and purified high molecular weight protein of non-typeable haemophilus which is antigenically related to the B. pertussis FHA, which may be obtained from natural sources or produced recombinantly.

A phage genomic library of a known strain of non-typeable Haemophilus was prepared by standard methods and the library was screened for clones expressing high molecular weight proteins, using a high titre antiserum against HMW's. A number of strongly reactive DNA clones were plaque-purified and sub-cloned into a T7 expression plasmid. It was found that they all expressed either one or the other of the two high-molecular-weight proteins designated HMW1 and HMW2, with apparent molecular weights of 125 and 120 kDa, respectively, encoded by open reading frames of 4.6 kb and 4.4 kb, respectively.

Representative clones expressing either HMW1 or HMW2 were further characterized and the genes isolated, purified and sequenced. The DNA sequence of HMW1 is shown in FIG. 1 and the corresponding derived amino acid sequence in FIG. 2. Similarly, the DNA sequence of HMW2 is shown in FIG. 3 and the corresponding derived amino acid sequence in FIG. 4. Partial purification of the isolated proteins and N-terminal sequence analysis indicated that the expressed proteins are truncated since their sequence starts at residue number 442 of both full length HMW1 and HMW2 gene products.

Subcloning studies with respect to the hmw1 and hmw2 genes indicated that correct processing of the HMW proteins required the products of additional downstream genes. It has been found that both the hmw1 and hmw2 genes are flanked by two additional downstream open reading frames (ORFs), designated b and c, respectively, (see FIGS. 6 and 7).

The b ORFs are 1635 bp in length, extending from nucleotides 5114 to 6748 in the case of hmw1 and nucleotides 5375 to 7009 in the case of hmw2, with their derived amino acid sequences 99% identical. The derived amino acid sequences demonstrate similarity with the derived amino acid sequences of two genes which encode proteins required for secretion and activation of hemolysins of P. mirabilis and S. marcescens.

The c ORFs are 1950 bp in length, extending from nucleotides 7062 to 9011 in the case of hmw1 and nucleotides 7249 to 9198 in the case of hmw2, with their derived amino acid sequences 96% identical. The hmw1 c ORF is preceded by a series of 9 bp direct tandem repeats. In plasmid subclones, interruption of the hmw1 b or c ORF results in defective processing and secretion of the hmw1 structural gene product.

The two high molecular weight proteins have been isolated and purified and shown to be partially protective against otitis media in chinchillas and to function as adhesins. These results indicate the potential for use of such high molecular proteins and structurally-related proteins of other non-typeable strains of Haemophilus influenzae as components in non-typeable Haemophilus influenzae vaccines.

Since the proteins provided herein are good cross-reactive antigens and are present in the majority of non-typeable Haemophilus strains, it is evident that these HMW proteins may become integral constituents of a universal Haemophilus vaccine. Indeed, these proteins may be used not only as protective antigens against otitis, sinusitis and bronchitis caused by the non-typeable Haemophilus strains, but also may be used as carriers for the protective Hib polysaccharides in a conjugate vaccine against meningitis. The proteins also may be used as carriers for other antigens, haptens and polysaccharides from other organisms, so as to induce immunity to such antigens, haptens and polysaccharides.

The nucleotide sequences encoding two high molecular weight proteins of a different non-typeable Haemophilus strain (designated HMW3 and HMW4) have been largely elucidated, and are presented in FIGS. 8 and 9. HMW3 has an apparent molecular weight of 125 kDa while HMW4 has an apparent molecular weight of 123 kDa. These high molecular weight proteins are antigenically related to the HMW1 and HMW2 proteins and to FHA. Sequence analysis of HMW3 is approximately 85% complete and of HMW4 95% complete, with short stretches at the 5'-ends of each gene remaining to be sequenced.

FIG. 10 contains a multiple sequence comparison of the derived amino acid sequences for the four high molecular weight proteins identified herein. As may be seen from this comparison, stretches of identical peptide sequence may be found throughout the length of the comparison, with HMW3 more closely resembling HMW1 and HMW4 more closely resembling HMW2. This information is highly suggestive of a considerable sequence homology between high molecular weight proteins from various non-typeable Haemophilus strains.

In addition, mutants of non-typeable H. influenzae strains that are deficient in expression of HMW1 or HMW2 or both have been constructed and examined for their capacity to adhere to cultured human epithelial cells. The hmw1 and hmw2 gene clusters have been expressed in E. coli and have been examined for in vitro adherence. The results of such experimentation demonstrate that both HMW1 and HMW2 mediate attachment and hence are adhesins and that this function is present even in the absence of other H. influenzae surface structures.

With the isolation and purification of the high molecular weight proteins, the inventors are able to determine the major protective epitopes by conventional epitope mapping and synthesize peptides corresponding to these determinants to be incorporated in fully synthetic or recombinant vaccines. Accordingly, the invention also comprises a synthetic peptide having an amino acid sequence corresponding to at least one protective epitope of a high molecular weight protein of a non-typeable Haemophilus influenzae. Such peptides are of varying length that constitute portions of the high-molecular-weight proteins, that can be used to induce immunity, either directly or as part of a conjugate, against the relative organisms and thus constitute vaccines for protection against the corresponding diseases.

The present invention also provides any variant or fragment of the proteins that retains the potential immunological ability to protect against disease caused by non-typeable Haemophilus strains. The variants may be constructed by partial deletions or mutations of the genes and expression of the resulting modified genes to give the protein variations.

EXAMPLES Example 1

Non-typeable H. influenzae strains 5 and 12 were isolated in pure culture from the middle ear fluid of children with acute otitis media. Chromosomal DNA from strain 12, providing genes encoding proteins HMW1 and HMW2, was prepared by preparing Sau3A partial restriction digests of chromosomal DNA and fractionating on sucrose gradients. Fractions containing DNA fragments in the 9 to 20 kbp range were pooled and a library was prepared by ligation into λEMBL3 arms. Ligation mixtures were packaged in vitro and plate-amplified in a P2 lysogen of E. coli LE392.

For plasmid subcloning studies, DNA from a representative recombinant phage was subcloned into the T7 expression plasmid pT7-7, containing the T7 RNA polymerase promoter Φ10, a ribosome-binding site and the translational start site for the T7 gene 10 protein upstream from a multiple cloning site (see FIG. 5B).

DNA sequence analysis was performed by the dideoxy method and both strands of the HMW1 gene and a single strand of the HMW2 gene were sequenced.

Western immunoblot analysis was performed to identify the recombinant proteins being produced by reactive phage clones. Phage lysates grown in LE392 cells or plaques picked directly from a lawn of LE392 cells on YT plates were solubilized in gel electrophoresis sample buffer prior to electrophoresis. Sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis was performed on 7.5% or 11% polyacrylamide modified Laemmli gels. After transfer of the proteins to nitrocellulose sheets, the sheets were probed sequentially with an E. coli-absorbed human serum sample containing high-titer antibody to the high-molecular-weight proteins and then with alkaline phosphatase-conjugated goat anti-human immunoglobulin G (IgG) second antibody. Sera from healthy adults contains high-titer antibody directed against surface-exposed high-molecular-weight proteins of non-typeable H. influenzae. One such serum sample was used as the screening antiserum after having been extensively absorbed with LE392 cells.

To identify recombinant proteins being produced by E. coli transformed with recombinant plasmids, the plasmids of interest were used to transform E. coli BL21 (DE3)/pLysS. The transformed strains were grown to an A₆₀₀ of 0.5 in L broth containing 50 μg of ampicillin per ml. IPTG was then added to 1 mM. One hour later, cells were harvested, and a sonicate of the cells was prepared. The protein concentrations of the samples were determined by the bicinchoninic acid method. Cell sonicates containing 100 μg of total protein were solubilized in electrophoresis sample buffer, subjected to SDS-polyacrylamide gel electrophoresis, and transferred to nitrocellulose. The nitrocellulose was then probed sequentially with the E. coli-absorbed adult serum sample and then with alkaline phosphatase-conjugated goat anti-human IgG second antibody.

Western immunoblot analysis also was performed to determine whether homologous and heterologous non-typeable H. influenzae strains expressed high-molecular-weight proteins antigenically related to the protein encoded by the cloned HMW1 gene (rHMW1). Cell sonicates of bacterial cells were solubilized in electrophoresis sample buffer, subjected to SDS-polyacrylamide gel electrophoresis, and transferred to nitrocellulose. Nitrocellulose was probed sequentially with polyclonal rabbit rHMW1 antiserum and then with alkaline phosphatase-conjugated goat anti-rabbit IgG second antibody.

Finally, Western immunoblot analysis was performed to determine whether non-typeable Haemophilus strains expressed proteins antigenically related to the filamentous hemagglutinin protein of Bordetella pertussis. Monoclonal antibody X3C, a murine immunoglobulin G (IgG) antibody which recognizes filamentous hemagglutinin, was used to probe cell sonicates by Western blot. An alkaline phosphatase-conjugated goat anti-mouse IgG second antibody was used for detection.

To generate recombinant protein antiserum, E. coli BL21(DE3)/pLysS was transformed with pHMW1-4, and expression of recombinant protein was induced with IPTG, as described above. A cell sonicate of the bacterial cells was prepared and separated into a supernatant and pellet fraction by centrifugation at 10,000×g for 30 min. The recombinant protein fractionated with the pellet fraction. A rabbit was subcutaneously immunized on biweekly schedule with 1 mg of protein from the pellet fraction, the first dose given with Freund's complete adjuvant and subsequent doses with Freund's incomplete adjuvant. Following the fourth injection, the rabbit was bled. Prior to use in the Western blot assay, the antiserum was absorbed extensively with sonicates of the host E. coli strain transformed with cloning vector alone.

To assess the sharing of antigenic determinants between HMW1 and filamentous hemagglutinin, enzyme-linked immunosorbent assay (ELISA) plates (Costar, Cambridge, Mass.) were coated with 60 μl of a 4-ug/ml solution of filamentous hemagglutinin in Dulbecco's phosphate-buffered saline per well for 2 h at room temperature. Wells were blocked for 1 h with 1% bovine serum albumin in Dulbecco's phosphate-buffered saline prior to addition of serum dilutions. rHMW1 antiserum was serially diluted in 0.1% Brij (Sigma, St. Louis, Mo.) in Dulbecco's phosphate-buffered saline and incubated for 3 h at room temperature. After being washed, the plates were incubated with peroxidase-conjugated goat anti-rabbit lgG antibody (Bio-Rad) for 2 h at room temperature and subsequently developed with 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (Sigma) at a concentration of 0.54 in mg/ml in 0.1M sodium citrate buffer, pH 4.2, containing 0.03% H₂ O₂. Absorbances were read on an automated ELISA reader.

Recombinant phage expressing HMW1 or HMW 2 were recovered as follows. The non-typeable H. influenzae strain 12 genomic library was screened for clones expressing high-molecular-weight proteins with an E. coli-absorbed human serum sample containing a high titer of antibodies directed against the high-molecular-weight proteins.

Numerous strongly reactive clones were identified along with more weakly reactive ones. Twenty strongly reactive clones were plaque-purified and examined by Western blot for expression of recombinant proteins. Each of the strongly reactive clones expressed one of two types of high-molecular-weight proteins, designated HMW1 and HMW2. The major immunoreactive protein bands in the HMW1 and HMW2 lysates migrated with apparent molecular masses of 125 and 120 kDa, respectively. In addition to the major bands, each lysate contained minor protein bands of higher apparent molecular weight. Protein bands seen in the HMW2 lysates at molecular masses of less than 120 kDa were not regularly observed and presumably represent proteolytic degradation products. Lysates of LE392 infected with the λEMBL3 cloning vector alone were non-reactive when immunologically screened with the same serum sample. Thus, the observed activity was not due to cross-reactive E. coli proteins or λEMBL3-encoded proteins. Furthermore, the recombinant proteins were not simply binding immunoglobulin nonspecifically, since the proteins were not reactive with the goat anti-human IgG conjugate alone, with normal rabbit sera, or with serum from a number of healthy young infants.

Representative clones expressing either the HMW1 or HMW2 recombinant proteins were characterized further. The restriction maps of the two phage types were different from each other, including the regions encoding the HMW1 and HMW2 structural genes. FIG. 5A shows restriction maps of representative recombinant phage which contained the HMW1 or HMW2 structural genes. The locations of the structural genes are indicated by the shaded bars.

HMW1 plasmid subclones were constructed by using the T7 expression plasmid T7-7 (FIGS. 5A and B). HMW2 plasmid subclones also were constructed, and the results with these latter subclones were similar to those observed with the HMW1 constructs.

The approximate location and direction of transcription of the HMW1 structure gene were initially determined by using plasmid pHMW1 (FIG. 5A). This plasmid was constructed by inserting the 8.5-kb BamHI-SalI fragment from λHMW1 into BamHI- and SalI-cut pT7-7. E. coli transformed with pHMW1 expressed an immunoreactive recombinant protein with an apparent molecular mass of 115 kDa, which was strongly inducible with IPTG. This protein was significantly smaller than the 125-kDa major protein expressed by the parent phage, indicating that it either was being expressed as a fusion protein or was truncated at the carboxy terminus.

To more precisely localize the 3' end of the structural gene, additional plasmids were constructed with progressive deletions from the 3' end of the pHMW1 construct. Plasmid pHMW1-1 was constructed by digestion of pHMW1 with PstI, isolation of the resulting 8.8-kb fragment, and religation. Plasmid pHMW1-2 was constructed by digestion of pHMW1 with HindIII, isolation of the resulting 7.5-kb fragment, and religation. E. coli transformed with either plasmid pHMW1-1 or pHMW1-2 also expressed an immunoreactive recombinant protein with an apparent molecular mass of 115 kDa. These results indicated that the 3' end of the structural gene was 5' of the HindIII site.

To more precisely localize the 5' end of the gene, plasmids pHMW1-4 and pHMW1-7 were constructed. Plasmid pHMW1-4 was constructed by cloning the 5.1-kb BamHI-HindIII fragment from λHMW1 into a pT7-7-derived plasmid containing the upstream 3.8-kb EcoRI-BamHi fragment. E. coli transformed with pHMW1-4 expressed an immunoreactive protein with an apparent molecular mass of approximately 160 kDa. Although protein production was inducible with IPTG, the levels of protein production in these transformants were substantially lower than those with the pHMW1-2 transformants described above. Plasmid pHMW1-7 was constructed by digesting pHMW1-4 with NdeI and SpeI. The 9.0-kbp fragment generated by this double digestion was isolated, blunt ended, and religated. E. coli transformed with pHMW1-7 also expressed an immunoreactive protein with an apparent molecular mass of 160 kDa, a protein identical in size to that expressed by the pHMW1-4 transformants. The result indicated that the initiation codon for the HMW1 structural gene was 3' of the SpeI site. DNA sequence analysis confirmed this conclusion.

As noted above, the λHMW1 phage clones expressed a major immunoreactive band of 125 kDa, whereas the HMW1 plasmid clones pHMW1-4 and pHMW1-7, which contained what was believed to be the full-length gene, expressed an immunoreactive protein of approximately 160 kDa. This size discrepancy was disconcerting. One possible explanation was that an additional gene or genes necessary for correct processing of the HMW1 gene product were deleted in the process of subcloning. To address this possibility, plasmid pHMW1-14 was constructed. This construct was generated by digesting pHMW1 with NdeI and MluI and inserting the 7.6-kbp NdeI-MluI fragment isolated from pHMW1-4. Such a construct would contain the full-length HMW1 gene as well as the DNA 3' of the HMW1 gene which was present in the original HMW1 phage. E. coli transformed with this plasmid expressed major immunoreactive proteins with apparent molecular masses of 125 and 160 kDa as well as additional degradation products. The 125- and 160-kDa bands were identical to the major and minor immunoreactive bands detected in the HMW1 phage lysates. Interestingly, the pHMW1-14 construct also expressed significant amounts of protein in the uninduced condition, a situation not observed with the earlier constructs.

The relationship between the 125- and 160-kDa proteins remains somewhat unclear. Sequence analysis, described below, reveals that the HMW1 gene would be predicted to encode a protein of 159 kDa. It is believed that the 160-kDa protein is a precursor form of the mature 125-kDa protein, with the conversion from one protein to the other being dependent on the products of the two downstream genes.

Sequence analysis of the HMW1 gene (FIG. 1) revealed a 4,608-bp open reading frame (ORF), beginning with an ATG codon at nucleotide 351 and ending with a TAG stop codon at nucleotide 4959. A putative ribosome-binding site with the sequence AGGAG begins 10 bp upstream of the putative initiation codon. Five other inframe ATG codons are located within 250 bp of the beginning of the ORF, but none of these is preceded by a typical ribosome-binding site. The 5'-flanking region of the ORF contains a series of direct tandem repeats, with the 7-bp sequence ATCTTTC repeated 16 times. These tandem repeats stop 100 bp 5' of the putative initiation codon. An 8-bp inverted repeat characteristic of a rho-independent transcriptional terminator is present, beginning at nucleotide 4983, 25 bp 3' of the presumed translational stop. Multiple termination codons are present in all three reading frames both upstream and downstream of the ORF. The derived amino acid sequence of the protein encoded by the HMW1 gene (FIG. 2) has a molecular weight of 159,000, in good agreement with the apparent molecular weights of the proteins expressed by the HMW1-4 and HMW1-7 transformants. The derived amino acid sequence of the amino terminus does not demonstrate the characteristics of a typical signal sequence. The BamHI site used in generation of pHMW1 comprises bp 1743 through 1748 of the nucleotide sequence. The ORF downstream of the BamHI site would be predicted to encode a protein of 111 kDa, in good agreement with the 115 kDa estimated for the apparent molecular mass of the pHMW1-encoded fusion protein.

The sequence of the HMW2 gene (FIG. 3) consists of a 4,431-bp ORF, beginning with an ATG codon at nucleotide 352 and ending with a TAG stop codon at nucleotide 4783. The first 1,259 bp of the ORF of the HMW2 gene are identical to those of the HMW1 gene. Thereafter, the sequences begin to diverge but are 80% identical overall. With the exception of a single base addition at nucleotide 93 of the HMW2 sequence, the 5'-flanking regions of the HMW1 and HMW2 genes are identical for 310 bp upstream from the respective initiation codons. Thus, the HMW2 gene is preceded by the same set of tandem repeats and the same putative ribosome-binding site which lies 5' of the HMW1 gene. A putative transcriptional terminator identical to that identified 3' of the HMW1 ORF is noted, beginning at nucleotide 4804. The discrepancy in the lengths of the two genes is principally accounted for by a 186-bp gap in the HMW2 sequence, beginning at nucleotide position 3839. The derived amino acid sequence of the protein encoded by the HMW2 gene (FIG. 4) has a molecular weight of 155,000 and is 71% identical with the derived amino acid sequence of the HMW1 gene.

The derived amino acid sequences of both the HMW1 and HMW2 genes (FIGS. 2 and 4) demonstrated sequence similarity with the derived amino acid sequence of filamentous hemagglutinin of Bordetella pertussis, a surface-associated protein of this organism. The initial and optimized TFASTA scores for the HMW1-filamentous hemagglutinin sequence comparison were 87 and 186, respectively, with a word size of 2. The z score for the comparison was 45.8. The initial and optimized TFASTA scores for the HMW2-filamentous hemagglutinin sequence comparison were 68 and 196, respectively. The z score for the latter comparison was 48.7. The magnitudes of the initial and optimized TFASTA scores and the z scores suggested that a biologically significant relationship existed between the HMW1 and HMW2 gene products and filamentous hemagglutinin. When the derived amino acid sequences of HMW1, HMW2, and filamentous hemagglutinin genes were aligned and compared, the similarities were most notable at the amino-terminal ends of the three sequences. Twelve of the first 22 amino acids in the predicted peptide sequences were identical. In additional, the sequences demonstrated a common five-amino-acid stretch, Asn-Pro-Asn-Gly-Ile, and several shorter stretches of sequence identity within the first 200 amino acids.

Example 2

To further explore the HMW1-filamentous hemagglutinin relationship, the ability of antiserum prepared against the HMW1-4 recombinant protein (rHMW1) to recognize purified filamentous hemagglutinin was assessed. The rHMW1 antiserum demonstrated ELISA reactivity with filamentous hemagglutinin in a dose-dependent manner. Preimmune rabbit serum had minimal reactivity in this assay. The rHMW1 antiserum also was examined in a Western blot assay and demonstrated weak but positive reactivity with purified filamentous hemagglutinin in this system also.

To identify the native Haemophilus protein corresponding to the HMW1 gene product and to determine the extent to which proteins antigenically related to the HMW1 cloned gene product were common among other non-typeable H. influenzae strains, a panel of Haemophilus strains was screened by Western blot with the rHMW1 antiserum. The antiserum recognized both a 125- and a 120-kDa protein band in the homologous strain 12, the putative mature protein products of the HMW1 and HMW2 genes, respectively.

When used to screen heterologous non-typeable H. influenzae strains, rHMW1 antiserum recognized high-molecular-weight proteins in 75% of 125 epidemiologically unrelated strains. In general, the antiserum reacted with one or two protein bands in the 100- to 150-kDa range in each of the heterologous strains in a pattern similar but not identical to that seen in the homologous strain.

Monoclonal antibody X3C is a murine IgG antibody directed against the filamentous hemagglutinin protein of B. pertussis. This antibody can inhibit the binding of B. pertussis cells to Chinese hamster ovary cells and HeLa cells in culture and will inhibit hemagglutination of erythrocytes by purified filamentous hemagglutinin. A Western blot assay was performed in which this monoclonal antibody was screened against the same panel of non-typeable H. influenzae strains discussed above. Monoclonal antibody X3C recognized both the high-molecular-weight proteins in non-typeable H. influenzae strain 12 which were recognized by the recombinant-protein antiserum. In addition, the monoclonal antibody recognized protein bands in a subset of heterologous non-typeable H. influenzae strains which were identical to those recognized by the recombinant-protein antiserum. On occasion, the filamentous hemagglutinin monoclonal antibody appeared to recognize only one of the two bands which had been recognized by the recombinant-protein antiserum. Overall, monoclonal antibody X3C recognized high-molecular-weight protein bands identical to those recognized by the rHMW1 antiserum in approximately 35% of our collection of non-typeable H. influenzae strains.

Example 3

Mutants deficient in expression of HMW1, MW2 or both proteins were constructed to examine the role of these proteins in bacterial adherence. The following strategy was employed. pHMW1-14 (see Example 1, FIG. 5A) was digested with BamHI and then ligated to a kanamycin cassette isolated on a 1.3-kb BamHl fragment from pUC4K. The resultant plasmid (pHMW1-17) was linearized by digestion with XbaI and transformed into non-typeable H. influenzae strain 12, followed by selection for kanamycin resistant colonies. Southern analysis of a series of these colonies demonstrated two populations of transformants, one with an insertion in the HMW1 structural gene and the other with an insertion in the HMW2 structural gene. One mutant from each of these classes was selected for further studies.

Mutants deficient in expression of both proteins were recovered using the following protocol. After deletion of the 2.1-kb fragment of DNA between two EcoRI sites spanning the 3'-portion of the HMW1 structural gene in pHMW-15, the kanamycin cassette from pUC4K was inserted as a 1.3-kb EcoRl fragment. The resulting plasmid (pHMW1-16) was linearized by digestion with XbaI and transformed into strain 12, followed again by selection for kanamycin resistant colonies. Southern analysis of a representative sampling of these colonies demonstrated that in seven of eight cases, insertion into both the HMW1 and HMW2 loci had occurred. One such mutant was selected for further studies.

To confirm the intended phenotypes, the mutant strains were examined by Western blot analysis with a polyclonal antiserum against recombinant HMW1 protein. The parental strain expressed both the 125-kD HMW1 and the 120-kD HMW2 protein. In contrast, the HMW2 mutant failed to express the 120-kD protein, and the HMW1 mutant failed to express the 125-kD protein. The double mutant lacked expression of either protein. On the basis of whole cell lysates, outer membrane profiles, and colony morphology, the wild type strain and the mutants were otherwise identical with one another. Transmission electron microscopy demonstrated that none of the four strains expressed pili.

The capacity of wild type strain 12 to adhere to Chang epithelial cells was examined. In such assays, bacteria were inoculated into broth and allowed to grow to a density of ˜2×10⁹ cfu/ml. Approximately 2×10⁷ cfu were inoculated onto epithelial cell monolayers, and plates were gently centrifuged at 165×g for 5 minutes to facilitate contact between bacteria and the epithelial surface. After incubation for 30 minutes at 37° C. in 5% CO₂, monolayers were rinsed 5 times with PBS to remove nonadherent organisms and were treated with trypsin-EDTA (0.05% trypsin, 0.5% EDTA) in PBS to release them from the plastic support. Well contents were agitated, and dilutions were plated on solid medium to yield the number of adherent bacteria per monolayer. Percent adherence was calculated by dividing the number of adherent cfu per monolayer by the number of inoculated cfu.

As depicted in Table 1 below (the Tables appear at the end of the descriptive text), this strain adhered quite efficiently, with nearly 90% of the inoculum binding to the monolayer. Adherence by the mutant expressing HMW1 but not HMW2 (HMW2⁻) was also quite efficient and comparable to that by the wild type strain. In contrast, attachment by the strain expressing HMW2 but deficient in expression of HMW1 (HMW1⁻) was decreased about 15-fold relative to the wild type. Adherence by the double mutant (HMW1⁻ /HMW2⁻) was decreased even further, approximately 50-fold compared with the wild type and approximately 3-fold compared with the HMW1 mutant. Considered together, these results suggest that both the HMW1 protein and the, HMW2 protein influence attachment to Chang epithelial cells. Interestingly, optimal adherence to this cell line appears to require HMW1 but not HMW2.

Example 4

Using the plasmids pHMW1-16 and pHMW1-17 (see Example 3) and following a scheme similar to that employed with strain 12 as described in Example 3, three non-typeable Haemophilus strain 5 mutants were isolated, including one with the kanamycin gene inserted into the hmw1-like (designated hmw3) locus, a second with an insertion in the hmw2-like (designated hmw4) locus, and a third with insertions in both loci. As predicted, Western immunoblot analysis demonstrated that the mutant with insertion of the kanamycin cassette into the hmw1-like locus had lost expression of the HMW3 125-kD protein, while the mutant with insertion into the hmw2-like locus failed to express the HMW4 123-kD protein. The mutant with a double insertion was unable to express either of the high molecular weight proteins.

As shown in Table 1 below, wild type strain 5 demonstrated high level adherence, with almost 80% of the inoculum adhering per monolayer. Adherence by the mutant deficient in expression of the HMW2-like protein was also quite high. In contrast, adherence by the mutant unable to express the, HMW1-like protein was reduced about 5-fold relative to the wild type, and attachment by the double mutant was diminished even further (approximately 25-fold). Examination of Giemsa-stained samples confirmed these observations (not shown). Thus, the results with strain 5 corroborate the findings with strain 12 and the HMW1 and HMW2 proteins.

Example 5

To confirm an adherence function for the HMW1 and HMW2 proteins and to examine the effect of HMW1 and HMW2 independently of other H. influenzae surface structures, the hmw1 and the hmw2 gene clusters were introduced into E. coli DH5α, using plasmids pHMW1-14 and pHMW2-21, respectively. As a control, the cloning vector, pT7-7, was also transformed into E. coli DH5α. Western blot analysis demonstrated that E. coli DH5α containing the hmw1 genes expressed a 125 kDa protein, while the same strain harboring the hmw2 genes expressed a 120-kDa protein. E. coli DH5α containing pT7-7 failed to react with antiserum against recombinant HMW1. Transmission electron microscopy revealed no pili or other surface appendages on any of the E. coli strains.

Adherence by the E. coli strains was quantitated and compared with adherence by wild type non-typeable H. influenzae strain 12. As shown in Table 2 below, adherence by E. coli DH5α containing vector alone was less than 1% of that for strain 12. In contrast, E. coli DH5α harboring the hmw1 gene cluster demonstrated adherence levels comparable to those for strain 12. Adherence by E. coli DH5α containing the hmw2 genes was approximately 6-fold lower than attachment by strain 12 but was increased 20-fold over adherence by E. coli DH5α with pT7-7 alone. These results indicate that the HMW1 and HMW2 proteins are capable of independently mediating attachment to Chang conjunctival cells. These results are consistent with the results with the H. influenzae mutants reported in Examples 3 and 4, providing further evidence that, with Chang epithelial cells, HMW1 is a more efficient adhesin than is HMW2.

Experiments with E. coli HB101 harboring pT7-7, pHMW1-14, or pHMW2-21 confirmed the results obtained with the DH5α derivatives (see Table 2).

Example 6

HMW1 and HMW2 were isolated and purified from non-typeable H. influenzae (NTHI) strain 12 in the following manner. Non-typeable Haemophilus bacteria from frozen stock culture were streaked onto a chocolate plate and grown overnight at 37° C. in an incubator with 5% CO₂. 50 ml starter culture of brain heart infusion (BHI) broth, supplemented with 10 μg/ml each of hemin and NAD was inoculated with growth on chocolate plate. The starter culture was grown until the optical density (O.D.-600 nm) reached 0.6 to 0.8 and then the bacteria in the starter culture was used to inoculate six 500 ml flasks of supplemented BHI using 8 to 10 ml per flask. The bacteria were grown in 500 ml flasks for an additional 5 to 6 hours at which time the O.D. was 1.5 or greater. Cultures were centrifuged at 10,000 rpm for 10 minutes.

Bacterial pellets were resuspended in a total volume of 250 ml of an extraction solution comprising 0.5M NaCl, 0.01M Na₂ EDTA, 0.01M Tris 50 μM 1,10-phenanthroline, pH 7.5. The cells were not sonicated or otherwise disrupted. The resuspended cells were allowed to sit on ice at 0° C. for 60 minutes. The resuspended cells were centrifuged at 10,000 rpm for 10 minutes at 4° C. to remove the majority of intact cells and cellular debris. The supernatant was collected and centrifuged at 100,000×g for 60 minutes at 4° C. The supernatant again was collected and dialyzed overnight at 4° C. against 0.01M sodium phosphate, pH 6.0.

The sample was centrifuged at 10,000 rpm for 10 minutes at 4° C. to remove insoluble debris precipitated from solution during dialysis. The supernatant was applied to a 10 ml CM Sepharose column which has been pre-equilibrated with 0.01M sodium phosphate, pH 6. Following application to this column, the column was washed with 0.01M sodium phosphate. Proteins were elevated from the column with a 0-0.5M KCl gradient in 0.01M Na phosphate, pH 6 and fractions were collected for gel examination. Coomassie gels of column fractions were carried out to identify those fractions containing high molecular weight proteins. The fractions containing high molecular weight proteins were pooled and concentrated to a 1 to 3 ml volume in preparation for application of sample to gel filtration column.

A Sepharose CL-4B gel filtration column was equilibrated with phosphate-buffered saline, pH 7.5. The concentrated high molecular weight protein sample was applied to the gel filtration column and column fractions were collected. Coomassie gels were performed an the column fractions to identify those containing high molecular weight proteins. The column fractions containing high molecular weight proteins were pooled.

The proteins were tested to determine whether they would protect against experimental otitis media caused by the homologous strain.

Chinchillas received three monthly subcutaneous injections with 40 μg of an HMW1-HMW2 protein mixture in Freund's adjuvant. One month after the last injection, the animals were challenged by intrabullar inoculation with 300 cfu of NTHI strain 12.

Infection developed in 5 of 5 control animals versus 5 of 10 immunized animals. Among infected animals, geometric mean bacterial counts in middle ear fluid 7 days post-challenge were 7.4×10⁶ in control animals verus 1.3×10⁵ in immunized animals.

Serum antibody titres following immunization were comparable in uninfected and infected animals. However, infection in immunized animals was uniformly associated with the appearance of bacteria down-regulated in expression of the HMW proteins, suggesting bacterial selection in response to immunologic pressure.

Although this data shows that protection following immunization was not complete, this data suggests the HMW adhesin proteins are potentially important protective antigens which may comprise one component of a multi-component NTHI vaccine.

These animal challenge tests were repeated in Chinchillas at a lower dose challenge than the 300 cfu employed above. In this instance, complete protection was achieved. In these experiments, groups of five animals were immunized with 20 μg of the HMW1-HMW2 mixture on days 1, 28, and 42 in the presence of AlPO₄. Blood samples were collected on day 53 to monitor the antibody response. On day 56, the left ear of animals was challenged with about 10 cfu of H. influenzae strain 12. Ear infection was monitored on day 4. Four animals in Group 3 were infected previously by H. influenzae strain 12 and were recovered completely for at least one month before the second challenge. The results are outlined in the following Table A:

                  TABLE A     ______________________________________     Protective ability of HMW protein against     non-typeable H. influenzae challenge in chinchilla model                     Number of Animals Showed                     Positive Ear Infection                                      Otosco-                                             cfu of                                      pic    Bac-     Group            Total    Tympano-                                      Examin-                                             teria/     (#)    Antigens  Animals  gram   ation  10 μL     ______________________________________     1      HMW       5        0      0      0     2      None      5        5      5      850-                                             3200                                             (4/5)     3      Convalescent                      4        0      0      0     ______________________________________

Example 7

A number of synthetic peptides were derived from HMW1. Antisera then was raised to these peptides. The anti-peptide antisera to peptide HMW1-P5 was shown to recognize HMW1. Peptide HMW1-P5 covers amino acids 1453 to 1481 of HMW1, has the sequence VDEVIEAKRILEKVKDLSDEEREALAKLG (SEQ ID NO:9), and represents bases 1498 to 1576 in FIG. 10.

This finding demonstrates that the DNA sequence and the derived protein is being interpreted in the correct reading frame and that peptides derived from the sequence can be produced which will be immunogenic.

SUMMARY OF DISCLOSURE

In summary of this disclosure, the present invention provides high molecular weight proteins of non-typeable Haemophilus, genes coding for the same and vaccines incorporating such proteins. Modifications are possible within the scope of this invention.

                  TABLE 1     ______________________________________     Effect of mutation of high molecular weight proteins on     adherence to Chang epithelial cells by nontypable H. influenzae.                 ADHERENCE*     Strain        % inoculum relative to wild type†     ______________________________________     Strain 12 derivatives     wild type     87.7 ± 5.9                              100.0 ± 6.7     HMW1-mutant   6.0 ± 0.9                              6.8 ± 1.0     HMW2-mutant   89.9 ± 10.8                              102.5 ± 12.3     HMW1-/HMW2-mutant                   2.0 ± 0.3                              2.3 ± 0.3     Strain 5 derivatives     wild type     78.7 ± 3.2                              100.0 ± 4.1     HMW1-like mutant                   15.7 ± 2.6                              19.9 ± 3.3     HMW2-like mutant                   103.7 ± 14.0                              131.7 ± 17.8     double mutant 3.5 ± 0.6                              4.4 ± 0.8     ______________________________________      *Numbers represent mean (± standard error of the mean) of measurements      in triplicate or quadruplicate from representative experiments.      †Adherence values for strain 12 derivatives are relative to strain      12 wild type; values for strain 5 derivatives are relative to strain 5      wild type.

                  TABLE 2     ______________________________________     Adherence by E. coli DH5α and HB101 harboring     hmw1 or hmw2 gene clusters.                    Adherence relative to     Strain*        H. influenzae strain 12†     ______________________________________     DH5α (pT7-7)                     0.7 ± 0.02     DH5α (pHMW1-14)                    114.2 ± 15.9     DH5α (pHMW2-21)                    14.0 ± 3.7     HB101 (pT7-7)  1.2 ± 0.5     HB101 (pHMW1-14)                    93.6 ± 15.8     HB101 (pHMW2-21)                    3.6 ± 0.9     ______________________________________      *The plasmid pHMW1-14 contains the hmw1 gene cluster, while pHMW2-21      contains the hmw2 gene cluster; pT7-7 is the cloning vector used in these      constructs.      †Numbers represent the mean (± standard error of the mean) of      measurements made in triplicate from representative experiments.

    __________________________________________________________________________     SEQUENCE LISTING     (1) GENERAL INFORMATION:     (iii) NUMBER OF SEQUENCES: 8     (2) INFORMATION FOR SEQ ID NO:1:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 5116 base pairs     (B) TYPE: nucleic acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: DNA (genomic)     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:     ACAGCGTTCTCTTAATACTAGTACAAACCCACAATAAAATATGACAAACAACAATTACAA60     CACCTTTTTTGCAGTCTATATGCAAATATTTTAAAAAATAGTATAAATCCGCCATATAAA120     ATGGTATAATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATC180     TTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTC240     ACATGCCCTGATGAACCGAGGGAAGGGAGGGAGGGGCAAGAATGAAGAGGGAGCTGAACG300     AACGCAAATGATAAAGTAATTTAATTGTTCAACTAACCTTAGGAGAAAATATGAACAAGC360     TATATCGTCTCAAATTCAGCAAACGCCTGAATGCTTTGGTTGCTGTGTCTGAATTGGCAC420     GGGGTTGTGACCATTCCACAGAAAAAGGCAGCGAAAAACCTGCTCGCATGAAAGTGCGTC480     ACTTAGCGTTAAAGCCACTTTCCGCTATGTTACTATCTTTAGGTGTAACATCTATTCCAC540     AATCTGTTTTAGCAAGCGGCTTACAAGGAATGGATGTAGTACACGGCACAGCCACTATGC600     AAGTAGATGGTAATAAAACCATTATCCGCAACAGTGTTGACGATATCATTAATTGGAAAC660     AATTTAACATCGACCAAAATGAAATGGTGCAGTTTTTACAAGAAAACAACAACTCCGCCG720     TATTCAACCGTGTTACATCTAACCAAATCTCCCAATTAAAAGGGATTTTAGATTCTAACG780     GACAAGTCTTTTTAATCAACCCAAATGGTATCACAATAGGTAAAGACGCAATTATTAACA840     CTAATGGCTTTACGGCTTCTACGCTAGACATTTCTAACGAAAACATCAAGGCGCGTAATT900     TCACCTTCGAGCAAACCAAAGATAAAGCGCTCGCTGAAATTGTGAATCACGGTTTAATTA960     CTGTCGGTAAAGACGGCAGTGTAAATCTTATTGGTGGCAAAGTGAAAAACGAGGGTGTGA1020     TTAGCGTAAATGGTGGCAGCATTTCTTTACTCGCAGGGCAAAAAATCACCATCAGCGATA1080     TAATAAACCCAACCATTACTTACAGCATTGCCGCGCCTGAAAATGAAGCGGTCAATCTGG1140     GCGATATTTTTGCCAAAGGCGGTAACATTAATGTCCGTGCTGCCACTATTCGAAACCAAG1200     GTAAACTTTCTGCTGATTCTGTAAGCAAAGATAAAAGCGGCAATATTGTTCTTTCCGCCA1260     AAGAGGGTGAAGCGGAAATTGGCGGTGTAATTTCCGCTCAAAATCAGCAAGCTAAAGGCG1320     GCAAGCTGATGATTACAGGCGATAAAGTCACATTAAAAACAGGTGCAGTTATCGACCTTT1380     CAGGTAAAGAAGGGGGAGAAACTTACCTTGGCGGTGACGAGCGCGGCGAAGGTAAAAAGG1440     GCATTCAATTAGCAAAGAAAACCTCTTTAGAAAAAGGCTCAACCATCAATGTATCAGGCA1500     AAGAAAAAGGCGGACGCGCTATTGTGTGGGGCGATATTGCGTTAATTGACGGCAATATTA1560     ACGCTCAAGGTAGTGGTGATATCGCTAAAACCGGTGGTTTTGTGGAGACGTCGGGGCATG1620     ATTTATTCATCAAAGACAATGCAATTGTTGACGCCAAAGAGTGGTTGTTAGACCCGGATA1680     ATGTATCTATTAATGCAGAAACAGCAGGACGCAGCAATACTTCAGAAGACGATGAATACA1740     CGGGATCCGGGAATAGTGCCAGCACCCCAAAACGAAACAAAGAAAAGACAACATTAACAA1800     ACACAACTCTTGAGAGTATACTAAAAAAAGGTACCTTTGTTAACATCACTGCTAATCAAC1860     GCATCTATGTCAATAGCTCCATTAATTTATCCAATGGCAGCTTAACTCTTTGGAGTGAGG1920     GTCGGAGCGGTGGCGGCGTTGAGATTAACAACGATATTACCACCGGTGATGATACCAGAG1980     GTGCAAACTTAACAATTTACTCAGGCGGCTGGGTTGATGTTCATAAAAATATCTCACTCG2040     GGGCGCAAGGTAACATAAACATTACAGCTAAACAAGATATCGCCTTTGAGAAAGGAAGCA2100     ACCAAGTCATTACAGGTCAAGGGACTATTACCTCAGGCAATCAAAAAGGTTTTAGATTTA2160     ATAATGTCTCTCTAAACGGCACTGGCAGCGGACTGCAATTCACCACTAAAAGAACCAATA2220     AATACGCTATCACAAATAAATTTGAAGGGACTTTAAATATTTCAGGGAAAGTGAACATCT2280     CAATGGTTTTACCTAAAAATGAAAGTGGATATGATAAATTCAAAGGACGCACTTACTGGA2340     ATTTAACCTCCTTAAATGTTTCCGAGAGTGGCGAGTTTAACCTCACTATTGACTCCAGAG2400     GAAGCGATAGTGCAGGCACACTTACCCAGCCTTATAATTTAAACGGTATATCATTCAACA2460     AAGACACTACCTTTAATGTTGAACGAAATGCAAGAGTCAACTTTGACATCAAGGCACCAA2520     TAGGGATAAATAAGTATTCTAGTTTGAATTACGCATCATTTAATGGAAACATTTCAGTTT2580     CGGGAGGGGGGAGTGTTGATTTCACACTTCTCGCCTCATCCTCTAACGTCCAAACCCCCG2640     GTGTAGTTATAAATTCTAAATACTTTAATGTTTCAACAGGGTCAAGTTTAAGATTTAAAA2700     CTTCAGGCTCAACAAAAACTGGCTTCTCAATAGAGAAAGATTTAACTTTAAATGCCACCG2760     GAGGCAACATAACACTTTTGCAAGTTGAAGGCACCGATGGAATGATTGGTAAAGGCATTG2820     TAGCCAAAAAAAACATAACCTTTGAAGGAGGTAACATCACCTTTGGCTCCAGGAAAGCCG2880     TAACAGAAATCGAAGGCAATGTTACTATCAATAACAACGCTAACGTCACTCTTATCGGTT2940     CGGATTTTGACAACCATCAAAAACCTTTAACTATTAAAAAAGATGTCATCATTAATAGCG3000     GCAACCTTACCGCTGGAGGCAATATTGTCAATATAGCCGGAAATCTTACCGTTGAAAGTA3060     ACGCTAATTTCAAAGCTATCACAAATTTCACTTTTAATGTAGGCGGCTTGTTTGACAACA3120     AAGGCAATTCAAATATTTCCATTGCCAAAGGAGGGGCTCGCTTTAAAGACATTGATAATT3180     CCAAGAATTTAAGCATCACCACCAACTCCAGCTCCACTTACCGCACTATTATAAGCGGCA3240     ATATAACCAATAAAAACGGTGATTTAAATATTACGAACGAAGGTAGTGATACTGAAATGC3300     AAATTGGCGGCGATGTCTCGCAAAAAGAAGGTAATCTCACGATTTCTTCTGACAAAATCA3360     ATATTACCAAACAGATAACAATCAAGGCAGGTGTTGATGGGGAGAATTCCGATTCAGACG3420     CGACAAACAATGCCAATCTAACCATTAAAACCAAAGAATTGAAATTAACGCAAGACCTAA3480     ATATTTCAGGTTTCAATAAAGCAGAGATTACAGCTAAAGATGGTAGTGATTTAACTATTG3540     GTAACACCAATAGTGCTGATGGTACTAATGCCAAAAAAGTAACCTTTAACCAGGTTAAAG3600     ATTCAAAAATCTCTGCTGACGGTCACAAGGTGACACTACACAGCAAAGTGGAAACATCCG3660     GTAGTAATAACAACACTGAAGATAGCAGTGACAATAATGCCGGCTTAACTATCGATGCAA3720     AAAATGTAACAGTAAACAACAATATTACTTCTCACAAAGCAGTGAGCATCTCTGCGACAA3780     GTGGAGAAATTACCACTAAAACAGGTACAACCATTAACGCAACCACTGGTAACGTGGAGA3840     TAACCGCTCAAACAGGTAGTATCCTAGGTGGAATTGAGTCCAGCTCTGGCTCTGTAACAC3900     TTACTGCAACCGAGGGCGCTCTTGCTGTAAGCAATATTTCGGGCAACACCGTTACTGTTA3960     CTGCAAATAGCGGTGCATTAACCACTTTGGCAGGCTCTACAATTAAAGGAACCGAGAGTG4020     TAACCACTTCAAGTCAATCAGGCGATATCGGCGGTACGATTTCTGGTGGCACAGTAGAGG4080     TTAAAGCAACCGAAAGTTTAACCACTCAATCCAATTCAAAAATTAAAGCAACAACAGGCG4140     AGGCTAACGTAACAAGTGCAACAGGTACAATTGGTGGTACGATTTCCGGTAATACGGTAA4200     ATGTTACGGCAAACGCTGGCGATTTAACAGTTGGGAATGGCGCAGAAATTAATGCGACAG4260     AAGGAGCTGCAACCTTAACTACATCATCGGGCAAATTAACTACCGAAGCTAGTTCACACA4320     TTACTTCAGCCAAGGGTCAGGTAAATCTTTCAGCTCAGGATGGTAGCGTTGCAGGAAGTA4380     TTAATGCCGCCAATGTGACACTAAATACTACAGGCACTTTAACTACCGTGAAGGGTTCAA4440     ACATTAATGCAACCAGCGGTACCTTGGTTATTAACGCAAAAGACGCTGAGCTAAATGGCG4500     CAGCATTGGGTAACCACACAGTGGTAAATGCAACCAACGCAAATGGCTCCGGCAGCGTAA4560     TCGCGACAACCTCAAGCAGAGTGAACATCACTGGGGATTTAATCACAATAAATGGATTAA4620     ATATCATTTCAAAAAACGGTATAAACACCGTACTGTTAAAAGGCGTTAAAATTGATGTGA4680     AATACATTCAACCGGGTATAGCAAGCGTAGATGAAGTAATTGAAGCGAAACGCATCCTTG4740     AGAAGGTAAAAGATTTATCTGATGAAGAAAGAGAAGCGTTAGCTAAACTTGGAGTAAGTG4800     CTGTACGTTTTATTGAGCCAAATAATACAATTACAGTCGATACACAAAATGAATTTGCAA4860     CCAGACCATTAAGTCGAATAGTGATTTCTGAAGGCAGGGCGTGTTTCTCAAACAGTGATG4920     GCGCGACGGTGTGCGTTAATATCGCTGATAACGGGCGGTAGCGGTCAGTAATTGACAAGG4980     TAGATTTCATCCTGCAATGAAGTCATTTTATTTTCGTATTATTTACTGTGTGGGTTAAAG5040     TTCAGTACGGGCTTTACCCATCTTGTAAAAAATTACGGAGAATACAATAAAGTATTTTTA5100     ACAGGTTATTATTATG5116     (2) INFORMATION FOR SEQ ID NO:2:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 1536 amino acids     (B) TYPE: amino acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: protein     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:     MetAsnLysIleTyrArgLeuLysPheSerLysArgLeuAsnAlaLeu     151015     ValAlaValSerGluLeuAlaArgGlyCysAspHisSerThrGluLys     202530     GlySerGluLysProAlaArgMetLysValArgHisLeuAlaLeuLys     354045     ProLeuSerAlaMetLeuLeuSerLeuGlyValThrSerIleProGln     505560     SerValLeuAlaSerGlyLeuGlnGlyMetAspValValHisGlyThr     65707580     AlaThrMetGlnValAspGlyAsnLysThrIleIleArgAsnSerVal     859095     AspAlaIleIleAsnTrpLysGlnPheAsnIleAspGlnAsnGluMet     100105110     ValGlnPheLeuGlnGluAsnAsnAsnSerAlaValPheAsnArgVal     115120125     ThrSerAsnGlnIleSerGlnLeuLysGlyIleLeuAspSerAsnGly     130135140     GlnValPheLeuIleAsnProAsnGlyIleThrIleGlyLysAspAla     145150155160     IleIleAsnThrAsnGlyPheThrAlaSerThrLeuAspIleSerAsn     165170175     GluAsnIleLysAlaArgAsnPheThrPheGluGlnThrLysAspLys     180185190     AlaLeuAlaGluIleValAsnHisGlyLeuIleThrValGlyLysAsp     195200205     GlySerValAsnLeuIleGlyGlyLysValLysAsnGluGlyValIle     210215220     SerValAsnGlyGlySerIleSerLeuLeuAlaGlyGlnLysIleThr     225230235240     IleSerAspIleIleAsnProThrIleThrTyrSerIleAlaAlaPro     245250255     GluAsnGluAlaValAsnLeuGlyAspIlePheAlaLysGlyGlyAsn     260265270     IleAsnValArgAlaAlaThrIleArgAsnGlnGlyLysLeuSerAla     275280285     AspSerValSerLysAspLysSerGlyAsnIleValLeuSerAlaLys     290295300     GluGlyGluAlaGluIleGlyGlyValIleSerAlaGlnAsnGlnGln     305310315320     AlaLysGlyGlyLysLeuMetIleThrGlyAspLysValThrLeuLys     325330335     ThrGlyAlaValIleAspLeuSerGlyLysGluGlyGlyGluThrTyr     340345350     LeuGlyGlyAspGluArgGlyGluGlyLysAsnGlyIleGlnLeuAla     355360365     LysLysThrSerLeuGluLysGlySerThrIleAsnValSerGlyLys     370375380     GluLysGlyGlyArgAlaIleValTrpGlyAspIleAlaLeuIleAsp     385390395400     GlyAsnIleAsnAlaGlnGlySerGlyAspIleAlaLysThrGlyGly     405410415     PheValGluThrSerGlyHisAspLeuPheIleLysAspAsnAlaIle     420425430     ValAspAlaLysGluTrpLeuLeuAspPheAspAsnValSerIleAsn     435440445     AlaGluThrAlaGlyArgSerAsnThrSerGluAspAspGluTyrThr     450455460     GlySerGlyAsnSerAlaSerThrProLysArgAsnLysGluLysThr     465470475480     ThrLeuThrAsnThrThrLeuGluSerIleLeuLysLysGlyThrPhe     485490495     ValAsnIleThrAlaAsnGlnArgIleTyrValAsnSerSerIleAsn     500505510     LeuSerAsnGlySerLeuThrLeuTrpSerGluGlyArgSerGlyGly     515520525     GlyValGluIleAsnAsnAspIleThrThrGlyAspAspThrArgGly     530535540     AlaAsnLeuThrIleTyrSerGlyGlyTrpValAspValHisLysAsn     545550555560     IleSerLeuGlyAlaGlnGlyAsnIleAsnIleThrAlaLysGlnAsp     565570575     IleAlaPheGluLysGlySerAsnGlnValIleThrGlyGlnGlyThr     580585590     IleThrSerGlyAsnGlnLysGlyPheArgPheAsnAsnValSerLeu     595600605     AsnGlyThrGlySerGlyLeuGlnPheThrThrLysArgThrAsnLys     610615620     TyrAlaIleThrAsnLysPheGluGlyThrLeuAsnIleSerGlyLys     625630635640     ValAsnIleSerMetValLeuProLysAsnGluSerGlyTyrAspLys     645650655     PheLysGlyArgThrTyrTrpAsnLeuThrSerLeuAsnValSerGlu     660665670     SerGlyGluPheAsnLeuThrIleAspSerArgGlySerAspSerAla     675680685     GlyThrLeuThrGlnProTyrAsnLeuAsnGlyIleSerPheAsnLys     690695700     AspThrThrPheAsnValGluArgAsnAlaArgValAsnPheAspIle     705710715720     LysAlaProIleGlyIleAsnLysTyrSerSerLeuAsnTyrAlaSer     725730735     PheAsnGlyAsnIleSerValSerGlyGlyGlySerValAspPheThr     740745750     LeuLeuAlaSerSerSerAsnValGlnThrProGlyValValIleAsn     755760765     SerLysTyrPheAsnValSerThrGlySerSerLeuArgPheLysThr     770775780     SerGlySerThrLysThrGlyPheSerIleGluLysAspLeuThrLeu     785790795800     AsnAlaThrGlyGlyAsnIleThrLeuLeuGlnValGluGlyThrAsp     805810815     GlyMetIleGlyLysGlyIleValAlaLysLysAsnIleThrPheGlu     820825830     GlyGlyAsnIleThrPheGlySerArgLysAlaValThrGluIleGlu     835840845     GlyAsnValThrIleAsnAsnAsnAlaAsnValThrLeuIleGlySer     850855860     AspPheAspAsnHisGlnLysProLeuThrIleLysLysAspValIle     865870875880     IleAsnSerGlyAsnLeuThrAlaGlyGlyAsnIleValAsnIleAla     885890895     GlyAsnLeuThrValGluSerAsnAlaAsnPheLysAlaIleThrAsn     900905910     PheThrPheAsnValGlyGlyLeuPheAspAsnLysGlyAsnSerAsn     915920925     IleSerIleAlaLysGlyGlyAlaArgPheLysAspIleAspAsnSer     930935940     LysAsnLeuSerIleThrThrAsnSerSerSerThrTyrArgThrIle     945950955960     IleSerGlyAsnIleThrAsnLysAsnGlyAspLeuAsnIleThrAsn     965970975     GluGlySerAspThrGluMetGlnIleGlyGlyAspValSerGlnLys     980985990     GluGlyAsnLeuThrIleSerSerAspLysIleAsnIleThrLysGln     99510001005     IleThrIleLysAlaGlyValAspGlyGluAsnSerAspSerAspAla     101010151020     ThrAsnAsnAlaAsnLeuThrIleLysThrLysGluLeuLysLeuThr     1025103010351040     GlnAspLeuAsnIleSerGlyPheAsnLysAlaGluIleThrAlaLys     104510501055     AspGlySerAspLeuThrIleGlyAsnThrAsnSerAlaAspGlyThr     106010651070     AsnAlaLysLysValThrPheAsnGlnValLysAspSerLysIleSer     107510801085     AlaAspGlyHisLysValThrLeuHisSerLysValGluThrSerGly     109010951100     SerAsnAsnAsnThrGluAspSerSerAspAsnAsnAlaGlyLeuThr     1105111011151120     IleAspAlaLysAsnValThrValAsnAsnAsnIleThrSerHisLys     112511301135     AlaValSerIleSerAlaThrSerGlyGluIleThrThrLysThrGly     114011451150     ThrThrIleAsnAlaThrThrGlyAsnValGluIleThrAlaGlnThr     115511601165     GlySerIleLeuGlyGlyIleGluSerSerSerGlySerValThrLeu     117011751180     ThrAlaThrGluGlyAlaLeuAlaValSerAsnIleSerGlyAsnThr     1185119011951200     ValThrValThrAlaAsnSerGlyAlaLeuThrThrLeuAlaGlySer     120512101215     ThrIleLysGlyThrGluSerValThrThrSerSerGlnSerGlyAsp     122012251230     IleGlyGlyThrIleSerGlyGlyThrValGluValLysAlaThrGlu     123512401245     SerLeuThrThrGlnSerAsnSerLysIleLysAlaThrThrGlyGlu     125012551260     AlaAsnValThrSerAlaThrGlyThrIleGlyGlyThrIleSerGly     1265127012751280     AsnThrValAsnValThrAlaAsnAlaGlyAspLeuThrValGlyAsn     128512901295     GlyAlaGluIleAsnAlaThrGluGlyAlaAlaThrLeuThrThrSer     130013051310     SerGlyLysLeuThrThrGluAlaSerSerHisIleThrSerAlaLys     131513201325     GlyGlnValAsnLeuSerAlaGlnAspGlySerValAlaGlySerIle     133013351340     AsnAlaAlaAsnValThrLeuAsnThrThrGlyThrLeuThrThrVal     1345135013551360     LysGlySerAsnIleAsnAlaThrSerGlyThrLeuValIleAsnAla     136513701375     LysAspAlaGluLeuAsnGlyAlaAlaLeuGlyAsnHisThrValVal     138013851390     AsnAlaThrAsnAlaAsnGlySerGlySerValIleAlaThrThrSer     139514001405     SerArgValAsnIleThrGlyAspLeuIleThrIleAsnGlyLeuAsn     141014151420     IleIleSerLysAsnGlyIleAsnThrValLeuLeuLysGlyValLys     1425143014351440     IleAspValLysTyrIleGlnProGlyIleAlaSerValAspGluVal     144514501455     IleGluAlaLysArgIleLeuGluLysValLysAspLeuSerAspGlu     146014651470     GluArgGluAlaLeuAlaLysLeuGlyValSerAlaValArgPheIle     147514801485     GluProAsnAsnThrIleThrValAspThrGlnAsnGluPheAlaThr     149014951500     ArgProLeuSerArgIleValIleSerGluGlyArgAlaCysPheSer     1505151015151520     AsnSerAspGlyAlaThrValCysValAsnIleAlaAspAsnGlyArg     152515301535     (2) INFORMATION FOR SEQ ID NO:3:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 4937 base pairs     (B) TYPE: nucleic acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: DNA (genomic)     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:     TAAATATACAAGATAATAAAAATAAATCAAGATTTTTGTGATGACAAACAACAATTACAA60     CACCTTTTTTGCAGTCTATATGCAAATATTTTAAAAAAATAGTATAAATCCGCCATATAA120     AATGGTATAATCTTTCATCTTTCATCTTTAATCTTTCATCTTTCATCTTTCATCTTTCAT180     CTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTT240     CACATGAAATGATGAACCGAGGGAAGGGAGGGAGGGGCAAGAATGAAGAGGGAGCTGAAC300     GAACGCAAATGATAAAGTAATTTAATTGTTCAACTAACCTTAGGAGAAAATATGAACAAG360     ATATATCGTCTCAAATTCAGCAAACGCCTGAATGCTTTGGTTGCTGTGTCTGAATTGGCA420     CGGGGTTGTGACCATTCCACAGAAAAAGGCTTCCGCTATGTTACTATCTTTAGGTGTAAC480     CACTTAGCGTTAAAGCCACTTTCCGCTATGTTACTATCTTTAGGTGTAACATCTATTCCA540     CAATCTGTTTTAGCAAGCGGCTTACAAGGAATGGATGTAGTACACGGCACAGCCACTATG600     CAAGTAGATGGTAATAAAACCATTATCCGCAACAGTGTTGACGCTATCATTAATTGGAAA660     CAATTTAACATCGACCAAAATGAAATGGTGCAGTTTTTACAAGAAAACAACAACTCCGCC720     GTATTCAACCGTGTTACATCTAACCAAATCTCCCAATTAAAAGGGATTTTAGATTCTAAC780     GGACAAGTCTTTTTAATCAACCCAAATGGTATCACAATAGGTAAAGACGCAATTATTAAC840     ACTAATGGCTTTACGGCTTCTACGCTAGACATTTCTAACGAAAACATCAAGGCGCGTAAT900     TTCACCTTCGAGCAAACCAAAGATAAAGCGCTCGCTGAAATTGTGAATCACGGTTTAATT960     ACTGTCGGTAAAGACGGCAGTGTAAATCTTATTGGTGGCAAAGTGAAAAACGAGGGTGTG1020     ATTAGCGTAAATGGTGGCAGCATTTCTTTACTCGCAGGGCAAAAAATCACCATCAGCGAT1080     ATAATAAACCCAACCATTACTTACAGCATTGCCGCGCCTGAAAATGAAGCGGTCAATCTG1140     GGCGATATTTTTGCCAAAGGCGGTAACATTAATGTCCGTGCTGCCACTATTCGAAACCAA1200     GGTAAACTTTCTGCTGATTCTGTAAGCAAAGATAAAAGCGGCAATATTGTTCTTTCCGCC1260     AAAGAGGGTGAAGCGGAAATTGGCGGTGTAATTTCCGCTCAAAATCAGCAAGCTAAAGGC1320     GGCAAGCTGATGATTACAGGCGATAAAGTCACATTAAAAACAGGTGCAGTTATCGACCTT1380     TCAGGTAAAGAAGGGGGAGAAACTTACCTTGGCGGTGACGAGCGCGGCGAAGGTAAAAAC1440     GGCATTCAATTAGCAAAGAAAACCTCTTTAGAAAAAGGCTCAACCATCAATGTATCAGGC1500     AAAGAAAAAGGCGGACGCGCTATTGTGTGGGGCGATATTGCGTTAATTGACGGCAATATT1560     AACGCTCAAGGTAGTGGTGATATCGCTAAAACCGGTGGTTTTGTGGAGACATCGGGGCAT1620     TATTTATCCATTGACAGCAATGCAATTGTTAAAACAAAAGAGTGGTTGCTAGACCCTGAT1680     GATGTAACAATTGAAGCCGAAGACCCCCTTCGCAATAATACCGGTATAAATGATGAATTC1740     CCAACAGGCACCGGTGAAGCAAGCGACCCTAAAAAAAATAGCGAACTCAAAACAACGCTA1800     ACCAATACAACTATTTCAAATTATCTGAAAAACGCCTGGACAATGAATATAACGGCATCA1860     AGAAAACTTACCGTTAATAGCTCAATCAACATCGGAAGCAACTCCCACTTAATTCTCCAT1920     AGTAAAGGTCAGCGTGGCGGAGGCGTTCAGATTGATGGAGATATTACTTCTAAAGGCGGA1980     AATTTAACCATTTATTCTGGCGGATGGGTTGATGTTCATAAAAATATTACGCTTGATCAG2040     GGTTTTTTAAATATTACCGCCGCTTCCGTAGCTTTTGAAGGTGGAAATAACAAAGCACGC2100     GACGCGGCAAATGCTAAAATTGTCGCCCAGGGCACTGTAACCATTACAGGAGAGGGAAAA2160     GATTTCAGGGCTAACAACGTATCTTTAAACGGAACGGGTAAAGGTCTGAATATCATTTCA2220     TCAGTGAATAATTTAACCCACAATCTTAGTGGCACAATTAACATATCTGGGAATATAACA2280     ATTAACCAAACTACGAGAAAGAACACCTCGTATTGGCAAACCAGCCATGATTCGCACTGG2340     AACGTCAGTGCTCTTAATCTAGAGACAGGCGCAAATTTTACCTTTATTAAATACATTTCA2400     AGCAATAGCAAAGGCTTAACAACACAGTATAGAAGCTCTGCAGGGGTGAATTTTAACGGC2460     GTAAATGGCAACATGTCATTCAATCTCAAAGAAGGAGCGAAAGTTAATTTCAAATTAAAA2520     CCAAACGAGAACATGAACACAAGCAAACCTTTACCAATTCGGTTTTTAGCCAATATCACA2580     GCCACTGGTGGGGGCTCTGTTTTTTTTGATATATATGCCAACCATTCTGGCAGAGGGGCT2640     GAGTTAAAAATGAGTGAAATTAATATCTCTAACGGCGCTAATTTTACCTTAAATTCCCAT2700     GTTCGCGGCGATGACGCTTTTAAAATCAACAAAGACTTAACCATAAATGCAACCAATTCA2760     AATTTCAGCCTCAGACAGACGAAAGATGATTTTTATGACGGGTACGCACGCAATGCCATC2820     AATTCAACCTACAACATATCCATTCTGGGCGGTAATGTCACCCTTGGTGGACAAAACTCA2880     AGCAGCAGCATTACGGGGAATATTACTATCGAGAAAGCAGCAAATGTTACGCTAGAAGCC2940     AATAACGCCCCTAATCAGCAAAACATAAGGGATAGAGTTATAAAACTTGGCAGCTTGCTC3000     GTTAATGGGAGTTTAAGTTTAACTGGCGAAAATGCAGATATTAAAGGCAATCTCACTATT3060     TCAGAAAGCGCCACTTTTAAAGGAAAGACTAGAGATACCCTAAATATCACCGGCAATTTT3120     ACCAATAATGGCACTGCCGAAATTAATATAACACAAGGAGTGGTAAAACTTGGCAATGTT3180     ACCAATGATGGTGATTTAAACATTACCACTCACGCTAAACGCAACCAAAGAAGCATCATC3240     GGCGGAGATATAATCAACAAAAAAGGAAGCTTAAATATTACAGACAGTAATAATGATGCT3300     GAAATCCAAATTGGCGGCAATATCTCGCAAAAAGAAGGCAACCTCACGATTTCTTCCGAT3360     AAAATTAATATCACCAAACAGATAACAATCAAAAAGGGTATTGATGGAGAGGACTCTAGT3420     TCAGATGCGACAAGTAATGCCAACCTAACTATTAAAACCAAAGAATTGAAATTGACAGAA3480     GACCTAAGTATTTCAGGTTTCAATAAAGCAGAGATTACAGCCAAAGATGGTAGAGATTTA3540     ACTATTGGCAACAGTAATGACGGTAACAGCGGTGCCGAAGCCAAAACAGTAACTTTTAAC3600     AATGTTAAAGATTCAAAAATCTCTGCTGACGGTCACAATGTGACACTAAATAGCAAAGTG3660     AAAACATCTAGCAGCAATGGCGGACGTGAAAGCAATAGCGACAACGATACCGGCTTAACT3720     ATTACTGCAAAAAATGTAGAAGTAAACAAAGATATTACTTCTCTCAAAACAGTAAATATC3780     ACCGCGTCGGAAAAGGTTACCACCACAGCAGGCTCGACCATTAACGCAACAAATGGCAAA3840     GCAAGTATTACAACCAAAACAGGTGATATCAGCGGTACGATTTCCGGTAACACGGTAAGT3900     GTTAGCGCGACTGGTGATTTAACCACTAAATCCGGCTCAAAAATTGAAGCGAAATCGGGT3960     GAGGCTAATGTAACAAGTGCAACAGGTACAATTGGCGGTACAATTTCCGGTAATACGGTA4020     AATGTTACGGCAAACGCTGGCGATTTAACAGTTGGGAATGGCGCAGAAATTAATGCGACA4080     GAAGGAGCTGCAACCTTAACCGCAACAGGGAATACCTTGACTACTGAAGCCGGTTCTAGC4140     ATCACTTCAACTAAGGGTCAGGTAGACCTCTTGGCTCAGAATGGTAGCATCGCAGGAAGC4200     ATTAATGCTGCTAATGTGACATTAAATACTACAGGCACCTTAACCACCGTGGCAGGCTCG4260     GATATTAAAGCAACCAGCGGCACCTTGGTTATTAACGCAAAAGATGCTAAGCTAAATGGT4320     GATGCATCAGGTGATAGTACAGAAGTGAATGCAGTCAACGCAAGCGGCTCTGGTAGTGTG4380     ACTGCGGCAACCTCAAGCAGTGTGAATATCACTGGGGATTTAAACACAGTAAATGGGTTA4440     AATATCATTTCGAAAGATGGTAGAAACACTGTGCGCTTAAGAGGCAAGGAAATTGAGGTG4500     AAATATATCCAGCCAGGTGTAGCAAGTGTAGAAGAAGTAATTGAAGCGAAACGCGTCCTT4560     GAAAAAGTAAAAGATTTATCTGATGAAGAAAGAGAAACATTAGCTAAACTTGGTGTAAGT4620     GCTGTACGTTTTGTTGAGCCAAATAATACAATTACAGTCAATACACAAAATGAATTTACA4680     ACCAGACCGTCAAGTCAAGTGATAATTTCTGAAGGTAAGGCGTGTTTCTCAAGTGGTAAT4740     GGCGCACGAGTATGTACCAATGTTGCTGACGATGGACAGCCGTAGTCAGTAATTGACAAG4800     GTAGATTTCATCCTGCAATGAAGTCATTTTATTTTCGTATTATTTACTGTGTGGGTTAAA4860     GTTCAGTACGGGCTTTACCCATCTTGTAAAAAATTACGGAGAATACAATAAAGTATTTTT4920     AACAGGTTATTATTATG4937     (2) INFORMATION FOR SEQ ID NO:4:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 1477 amino acids     (B) TYPE: amino acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: protein     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:     MetAsnLysIleTyrArgLeuLysPheSerLysArgLeuAsnAlaLeu     151015     ValAlaValSerGluLeuAlaArgGlyCysAspHisSerThrGluLys     202530     GlySerGluLysProAlaArgMetLysValArgHisLeuAlaLeuLys     354045     ProLeuSerAlaMetLeuLeuSerLeuGlyValThrSerIleProGln     505560     SerValLeuAlaSerGlyLeuGlnGlyMetAspValValHisGlyThr     65707580     AlaThrMetGlnValAspGlyAsnLysThrIleIleArgAsnSerVal     859095     AspAlaIleIleAsnTrpLysGlnPheAsnIleAspGlnAsnGluMet     100105110     ValGlnPheLeuGlnGluAsnAsnAsnSerAlaValPheAsnArgVal     115120125     ThrSerAsnGlnIleSerGlnLeuLysGlyIleLeuAspSerAsnGly     130135140     GlnValPheLeuIleAsnProAsnGlyIleThrIleGlyLysAspAla     145150155160     IleIleAsnThrAsnGlyPheThrAlaSerThrLeuAspIleSerAsn     165170175     GluAsnIleLysAlaArgAsnPheThrPheGluGlnThrLysAspLys     180185190     AlaLeuAlaGluIleValAsnHisGlyLeuIleThrValGlyLysAsp     195200205     GlySerValAsnLeuIleGlyGlyLysValLysAsnGluGlyValIle     210215220     SerValAsnGlyGlySerIleSerLeuLeuAlaGlyGlnLysIleThr     225230235240     IleSerAspIleIleAsnProThrIleThrTyrSerIleAlaAlaPro     245250255     GluAsnGluAlaValAsnLeuGlyAspIlePheAlaLysGlyGlyAsn     260265270     IleAsnValArgAlaAlaThrIleArgAsnGlnGlyLysLeuSerAla     275280285     AspSerValSerLysAspLysSerGlyAsnIleValLeuSerAlaLys     290295300     GluGlyGluAlaGluIleGlyGlyValIleSerAlaGlnAsnGlnGln     305310315320     AlaLysGlyGlyLysLeuMetIleThrGlyAspLysValThrLeuLys     325330335     ThrGlyAlaValIleAspLeuSerGlyLysGluGlyGlyGluThrTyr     340345350     LeuGlyGlyAspGluArgGlyGluGlyLysAsnGlyIleGlnLeuAla     355360365     LysLysThrSerLeuGluLysGlySerThrIleAsnValSerGlyLys     370375380     GluLysGlyGlyPheAlaIleValTrpGlyAspIleAlaLeuIleAsp     385390395400     GlyAsnIleAsnAlaGlnGlySerGlyAspIleAlaLysThrGlyGly     405410415     PheValGluThrSerGlyHisAspLeuPheIleLysAspAsnAlaIle     420425430     ValAspAlaLysGluTrpLeuLeuAspPheAspAsnValSerIleAsn     435440445     AlaGluAspProLeuPheAsnAsnThrGlyIleAsnAspGluPhePro     450455460     ThrGlyThrGlyGluAlaSerAspProLysLysAsnSerGluLeuLys     465470475480     ThrThrLeuThrAsnThrThrIleSerAsnTyrLeuLysAsnAlaTrp     485490495     ThrMetAsnIleThrAlaSerArgLysLeuThrValAsnSerSerIle     500505510     AsnIleGlySerAsnSerHisLeuIleLeuHisSerLysGlyGlnArg     515520525     GlyGlyGlyValGlnIleAspGlyAspIleThrSerLysGlyGlyAsn     530535540     LeuThrIleTyrSerGlyGlyTrpValAspValHisLysAsnIleThr     545550555560     LeuAspGlnGlyPheLeuAsnIleThrAlaAlaSerValAlaPheGlu     565570575     GlyGlyAsnAsnLysAlaArgAspAlaAlaAsnAlaLysIleValAla     580585590     GlnGlyThrValThrIleThrGlyGluGlyLysAspPheArgAlaAsn     595600605     AsnValSerLeuAsnGlyThrGlyLysGlyLeuAsnIleIleSerSer     610615620     ValAsnAsnLeuThrHisAsnLeuSerGlyThrIleAsnIleSerGly     625630635640     AsnIleThrIleAsnGlnThrThrArgLysAsnThrSerTyrTrpGln     645650655     ThrSerHisAspSerHisTrpAsnValSerAlaLeuAsnLeuGluThr     660665670     GlyAlaAsnPheThrPheIleLysTyrIleSerSerAsnSerLysGly     675680685     LeuThrThrGlnTyrArgSerSerAlaGlyValAsnPheAsnGlyVal     690695700     AsnGlyAsnMetSerPheAsnLeuLysGluGlyAlaLysValAsnPhe     705710715720     LysLeuLysProAsnGluAsnMetAsnThrSerLysProLeuProIle     725730735     ArgPheLeuAlaAsnIleThrAlaThrGlyGlyGlySerValPhePhe     740745750     AspIleTyrAlaAsnHisSerGlyArgGlyAlaGluLeuLysMetSer     755760765     GluIleAsnIleSerAsnGlyAlaAsnPheThrLeuAsnSerHisVal     770775780     ArgGlyAspAspAlaPheLysIleAsnLysAspLeuThrIleAsnAla     785790795800     ThrAsnSerAsnPheSerLeuArgGlnThrLysAspAspPheTyrAsp     805810815     GlyTyrAlaArgAsnAlaIleAsnSerThrTyrAsnIleSerIleLeu     820825830     GlyGlyAsnValThrLeuGlyGlyGlnAsnSerSerSerSerIleThr     835840845     GlyAsnIleThrIleGluLysAlaAlaAsnValThrLeuGluAlaAsn     850855860     AsnAlaProAsnGlnGlnAsnIleArgAspArgValIleLysLeuGly     865870875880     SerLeuLeuValAsnGlySerLeuSerLeuThrGlyGluAsnAlaAsp     885890895     IleLysGlyAsnLeuThrIleSerGluSerAlaThrPheLysGlyLys     900905910     ThrArgAspThrLeuAsnIleThrGlyAsnPheThrAsnAsnGlyThr     915920925     AlaGluIleAsnIleThrGlnGlyValValLysLeuGlyAsnValThr     930935940     AsnAspGlyAspLeuAsnIleThrThrHisAlaLysArgAsnGlnArg     945950955960     SerIleIleGlyGlyAspIleIleAsnLysLysGlySerLeuAsnIle     965970975     ThrAspSerAsnAsnAspAlaGluIleGlnIleGlyGlyAsnIleSer     980985990     GlnLysGluGlyAsnLeuThrIleSerSerAspLysIleAsnIleThr     99510001005     LysGlnIleThrIleLysLysGlyIleAspGlyGluAspSerSerSer     101010151020     AspAlaThrSerAsnAlaAsnLeuThrIleLysThrLysGluLeuLys     1025103010351040     LeuThrGluAspLeuSerIleSerGlyPheAsnLysAlaGluIleThr     104510501055     AlaLysAspGlyArgAspLeuThrIleGlyAsnSerAsnAspGlyAsn     106010651070     SerGlyAlaGluAlaLysThrValThrPheAsnAsnValLysAspSer     107510801085     LysIleSerAlaAspGlyHisAsnValThrLeuAsnSerLysValLys     109010951100     ThrSerSerSerAsnGlyGlyArgGluSerAsnSerAspAsnAspThr     1105111011151120     GlyLeuThrIleThrAlaLysAsnValGluValAsnLysAspIleThr     112511301135     SerLeuLysThrValAsnIleThrAlaSerGluLysValThrThrThr     114011451150     AlaGlySerThrIleAsnAlaThrAsnGlyLysAlaSerIleThrThr     115511601165     LysThrGlyAspIleSerGlyThrIleSerGlyAsnThrValSerVal     117011751180     SerAlaThrValAspLeuThrThrLysSerGlySerLysIleGluAla     1185119011951200     LysSerGlyGluAlaAsnValThrSerAlaThrGlyThrIleGlyGly     120512101215     ThrIleSerGlyAsnThrValAsnValThrAlaAsnAlaGlyAspLeu     122012251230     ThrValGlyAsnGlyAlaGluIleAsnAlaThrGluGlyAlaAlaThr     123512401245     LeuThrAlaThrGlyAsnThrLeuThrThrGluAlaGlySerSerIle     125012551260     ThrSerThrLysGlyGlnValAspLeuLeuAlaGlnAsnGlySerIle     1265127012751280     AlaGlySerIleAsnAlaAlaAsnValThrLeuAsnThrThrGlyThr     128512901295     LeuThrThrValAlaGlySerAspIleLysAlaThrSerGlyThrLeu     130013051310     ValIleAsnAlaLysAspAlaLysLeuAsnGlyAspAlaSerGlyAsp     131513201325     SerThrGluValAsnAlaValAsnAlaSerGlySerGlySerValThr     133013351340     AlaAlaThrSerSerSerValAsnIleThrGlyAspLeuAsnThrVal     1345135013551360     AsnGlyLeuAsnIleIleSerLysAspGlyArgAsnThrValArgLeu     136513701375     ArgGlyLysGluIleGluValLysTyrIleGlnProGlyValAlaSer     138013851390     ValGluGluValIleGluAlaLysArgValLeuGluLysValLysAsp     139514001405     LeuSerAspGluGluArgGluThrLeuAlaLysLeuGlyValSerAla     141014151420     ValArgPheValGluProAsnAsnThrIleThrValAsnThrGlnAsn     1425143014351440     GluPheThrThrArgProSerSerGlnValIleIleSerGluGlyLys     144514501455     AlaCysPheSerSerGlyAsnGlyAlaArgValCysThrAsnValAla     146014651470     AspAspGlyGlnPro     1475     (2) INFORMATION FOR SEQ ID NO:5:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 9171 base pairs     (B) TYPE: nucleic acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: DNA (genomic)     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:     ACAGCGTTCTCTTAATACTAGTACAAACCCACAATAAAATATGACAAACAACAATTACAA60     CACCTTTTTTGCAGTCTATATGCAAATATTTTAAAAAATAGTATAAATCCGCCATATAAA120     ATGGTATAATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATC180     TTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTC240     ACATGAAATGATGAACCGAGGGAAGGGAGGGAGGGGCAAGAATGAAGAGGGAGCTGAACG300     AACGCAAATGATAAAGTAATTTAATTGTTCAACTAACCTTAGGAGAAAATATGAACAAGA360     TATATCGTCTCAAATTCAGCAAACGCCTGAATGCTTTGGTTGCTGTGTCTGAATTGGCAC420     GGGGTTGTGACCATTCCACAGAAAAAGGCAGCGAAAAACCTGCTCGCATGAAAGTGCGTC480     ACTTAGCGTTAAAGCCACTTTCCGCTATGTTACTATCTTTAGGTGTAACATCTATTCCAC540     AATCTGTTTTAGCAAGCGGCTTACAAGGAATGGATGTAGTACACGGCACAGCCACTATGC600     AAGTAGATGGTAATAAAACCATTATCCGCAACAGTGTTGACGCTATCATTAATTGGAAAC660     AATTTAACATCGACCAAAATGAAATGGTGCAGTTTTTACAAGAAAACAACAACTCCGCCG720     TATTCAACCGTGTTACATCTAACCAAATCTCCCAATTAAAAGGGATTTTAGATTCTAACG780     GACAAGTCTTTTTAATCAACCCAAATGGTATCACAATAGGTAAAGACGCAATTATTAACA840     CTAATGGCTTTACGGCTTCTACGCTAGACATTTCTAACGAAAACATCAAGGCGCGTAATT900     TCACCTTCGAGCAAACCAAAGATAAAGCGCTCGCTGAAATTGTGAATCACGGTTTAATTA960     CTGTCGGTAAAGACGGCAGTGTAAATCTTATTGGTGGCAAAGTGAAAAACGAGGGTGTGA1020     TTAGCGTAAATGGTGGCAGCATTTCTTTACTCGCAGGGCAAAAAATCACCATCAGCGATA1080     TAATAAACCCAACCATTACTTACAGCATTGCCGCGCCTGAAAATGAAGCGGTCAATCTGG1140     GCGATATTTTTGCCAAAGGCGGTAACATTAATGTCCGTGCTGCCACTATTCGAAACCAAG1200     CTTTCCGCCAAAGAGGGTGAAGCGGAAATTGGCGGTGTAATTTCCGCTCAAAATCAGCAA1260     GCTAAAGGCGGCAAGCTGATGATTACAGGCGATAAAGTCACATTAAAAACAGGTGCAGTT1320     ATCGACCTTTCAGGTAAAGAAGGGGGAGAAACTTACCTTGGCGGTGACGAGCGCGGCGAA1380     GGTAAAAACGGCATTCAATTAGCAAAGAAAACCTCTTTAGAAAAAGGCTCAACCATCAAT1440     GTATCAGGCAAAGAAAAAGGCGGACGCGCTATTGTGTGGGGCGATATTGCGTTAATTGAC1500     GGCAATATTAACGCTCAAGGTAGTGGTGATATCGCTAAAACCGGTGGTTTTGTGGAGACG1560     TCGGGGCATGATTTATTCATCAAAGACAATGCAATTGTTGACGCCAAAGAGTGGTTGTTA1620     GACCCGGATAATGTATCTATTAATGCAGAAACAGCAGGACGCAGCAATACTTCAGAAGAC1680     GATGAATACACGGGATCCGGGAATAGTGCCAGCACCCCAAAACGAAACAAAGAAAAGACA1740     ACATTAACAAACACAACTCTTGAGAGTATACTAAAAAAAGGTACCTTTGTTAACATCACT1800     GCTAATCAACGCATCTATGTCAATAGCTCCATTAATTTATCCAATGGCAGCTTAACTCTT1860     TGGAGTGAGGGTCGGAGCGGTGGCGGCGTTGAGATTAACAACGATATTACCACCGGTGAT1920     GATACCAGAGGTGCAAACTTAACAATTTACTCAGGCGGCTGGGTTGATGTTCATAAAAAT1980     ATCTCACTCGGGGCGCAAGGTAACATAAACATTACAGCTAAACAAGATATCGCCTTTGAG2040     AAAGGAAGCAACCAAGTCATTACAGGTCAAGGGACTATTACCTCAGGCAATCAAAAAGGT2100     TTTAGATTTAATAATGTCTCTCTAAACGGCACTGGCAGCGGACTGCAATTCACCACTAAA2160     AGAACCAATAAATACGCTATCACAAATAAATTTGAAGGGACTTTAAATATTTCAGGGAAA2220     GTGAACATCTCAATGGTTTTACCTAAAAATGAAAGTGGATATGATAAATTCAAAGGACGC2280     ACTTACTGGAATTTAACCTCGAAAGTGGATATGATAAATTCAAAGGACGCCCTCACTATT2340     GACTCCAGAGGAAGCGATAGTGCAGGCACACTTACCCAGCCTTATAATTTAAACGGTATA2400     TCATTCAACAAAGACACTACCTTTAATGTTGAACGAAATGCAAGAGTCAACTTTGACATC2460     AAGGCACCAATAGGGATAAATAAGTATTCTAGTTTGAATTACGCATCATTTAATGGAAAC2520     ATTTCAGTTTCGGGAGGGGGGAGTGTTGATTTCACACTTCTCGCCTCATCCTCTAACGTC2580     CAAACCCCCGGTGTAGTTATAAATTCTAAATACTTTAATGTTTCAACAGGGTCAAGTTTA2640     AGATTTAAAACTTCAGGCTCAACAAAAACTGGCTTCTCAATAGAGAAAGATTTAACTTTA2700     AATGCCACCGGAGGCAACATAACACTTTTGCAAGTTGAAGGCACCGATGGAATGATTGGT2760     AAAGGCATTGTAGCCAAAAAAAACATAACCTTTGAAGGAGGTAAGATGAGGTTTGGCTCC2820     AGGAAAGCCGTAACAGAAATCGAAGGCAATGTTACTATCAATAACAACGCTAACGTCACT2880     CTTATCGGTTCGGATTTTGACAACCATCAAAAACCTTTAACTATTAAAAAAGATGTCATC2940     ATTAATAGCGGCAACCTTACCGCTGGAGGCAATATTGTCAATATAGCCGGAAATCTTACC3000     GTTGAAAGTAACGCTAATTTCAAAGCTATCACAAATTTCACTTTTAATGTAGGCGGCTTG3060     TTTGACAACAAAGGCAATTCAAATATTTCCATTGCCAAAGGAGGGGCTCGCTTTAAAGAC3120     ATTGATAATTCCAAGAATTTAAGCATCACCACCAACTCCAGCTCCACTTACCGCACTATT3180     ATAAGCGGCAATATAACCAATAAAAACGGTGATTTAAATATTACGAACGAAGGTAGTGAT3240     ACTGAAATGCAAATTGGCGGCGATGTCTCGCAAAAAGAAGGTAATCTCACGATTTCTTCT3300     GACAAAATCAATATTACCAAACAGATAACAATCAAGGCAGGTGTTGATGGGGAGAATTCC3360     GATTCAGACGCGACAAACAATGCCAATCTAACCATTAAAACCAAAGAATTGAAATTAACG3420     CAAGACCTAAATATTTCAGGTTTCAATAAAGCAGAGATTACAGCTAAAGATGGTAGTGAT3480     TTAACTATTGGTAACACCAATAGTGCTGATGGTACTAATGCCAAAAAAGTAACCTTTAAC3540     CAGGTTAAAGATTCAAAAATCTCTGCTGACGGTCACAAGGTGACACTACACAGCAAAGTG3600     GAAACATCCGGTAGTAATAACAACACTGAAGATAGCAGTGACAATAATGCCGGCTTAACT3660     ATCGATGCAAAAAATGTAACAGTAAACAACAATATTACTTCTCACAAAGCAGTGAGCATC3720     TCTGCGACAAGTGGAGAAATTACCACTAAAACAGGTACAACCATTAACGCAACCACTGGT3780     AACGTGGAGATAACCGCTCAAACAGGTAGTATCCTAGGTGGAATTGAGTCCAGCTCTGGC3840     TCTGTAACACTTACTGCAACCGAGGGCGCTCTTGCTGTAAGCAATATTTCGGGCAACACC3900     GTTACTGTTACTGCAAATAGCGGTGCATTAACCACTTTGGCAGGCTCTACAATTAAAGGA3960     ACCGAGAGTGTAACCACTTCAAGTCAATCAGGCGATATCGGCGGTACGATTTCTGGTGGC4020     ACAGTAGAGGTTAAAGCAACCGAAAGTTTAACCACTCAATCCAATTCAAAAATTAAAGCA4080     ACAACAGGCGAGGCTAACGTAACAAGTGCAACAGGTACAATTGGTGGTACGATTTCCGGT4140     AATACGGTAAATGTTACGGCAAACGCTGGCGATTTAACAGTTGGGAATGGCGCAGAAATT4200     AATGCGACAGAAGGAGCTGCAACCTTAACTACATCATCGGGCAAATTAACTACCGAAGCT4260     AGTTCACACATTACTTCAGCCAAGGGTCAGGTAAATCTTTCAGCTCAGGATGGTAGCGTT4320     GCAGGAAGTATTAATGCCGCCAATGTGACACTAAATACTACAGGCACTTTAACTACCGTG4380     AAGGGTTCAAACATTAATGCAACCAGCGGTACCTTGGTTATTAACGCAAAAGACGCTGAG4440     CTAAATGGCGCAGCATTGGGTAACCACACAGTGGTAAATGCAACCAACGCAAATGGCTCC4500     GGCAGCGTAATCGCGACAACCTCAAGCAGAGTGAACATCACTGGGGATTTAATCACAATA4560     AATGGATTAAATATCATTTCAAAAAACGGTATAAACACCGTACTGTTAAAAGGCGTTAAA4620     ATTGATGTGAAATACATTCAACCGGGTATAGCAAGCGTAGATGAAGTAATTGAAGCGAAA4680     CGCATCCTTGAGAAGGTAAAAGATTTATCTGATGAAGAAAGAGAAGCGTTAGCTAAACTT4740     GGCGTAAGTGCTGTACGTTTTATTGAGCCAAATAATACAATTACAGTCGATACACAAAAT4800     GAATTTGCAACCAGACCATTAAGTCGAATAGTGATTTCTGAAGGCAGGGCGTGTTTCTCA4860     AACAGTGATGGCGCGACGGTGTGCGTTAATATCGCTGATAACGGGCGGTAGCGGTCAGTA4920     ATTGACAAGGTAGATTTCATCCTGCAATGAAGTCATTTTATTTTCGTATTATTTACTGTG4980     TGGGTTAAAGTTCAGTACGGGCTTTACCCATCTTGTAAAAAATTACGGAGAATACAATAA5040     AGTATTTTTAACAGGTTATTATTATGAAAAATATAAAAAGCAGATTAAAACTCAGTGCAA5100     TATCAGTATTGCTTGGCCTGGCTTCTTCATCATTGTATGCAGAAGAAGCGTTTTTAGTAA5160     AAGGCTTTCAGTTATCTGGTGCACTTGAAACTTTAAGTGAAGACGCCCAACTGTCTGTAG5220     CAAAATCTTTATCTAAATACCAAGGCTCGCAAACTTTAACAAACCTAAAAACAGCACAGC5280     TTGAATTACAGGCTGTGCTAGATAAGATTGAGCCAAATAAGTTTGATGTGATATTGCCAC5340     AACAAACCATTACGGATGGCAATATTATGTTTGAGCTAGTCTCGAAATCAGCCGCAGAAA5400     GCCAAGTTTTTTATAAGGCGAGCCAGGGTTATAGTGAAGAAAATATCGCTCGTAGCCTGC5460     CATCTTTGAAACAAGGAAAAGTGTATGAAGATGGTCGTCAGTGGTTCGATTTGCGTGAAT5520     TCAATATGGCAAAAGAAAATCCACTTAAAGTCACTCGCGTGCATTACGAGTTAAACCCTA5580     AAAACAAAACCTCTGATTTGGTAGTTGCAGGTTTTTCGCCTTTTGGCAAAACGCGTAGCT5640     TTGTTTCCTATGATAATTTCGGCGCAAGGGAGTTTAACTATCAACGTGTAAGTCTAGGTT5700     TTGTAAATGCCAATTTGACCGGACATGATGATGTATTAAATCTAAACGCATTGACCAATG5760     TAAAAGCACCATCAAAATCTTATGCGGTAGGCATAGGATATACTTATCCGTTTTATGATA5820     AACACCAATCCTTAAGTCTTTATACCAGCATGAGTTATGCTGATTCTAATGATATCGACG5880     GCTTACCAAGTGCGATTAATCGTAAATTATCAAAAGGTCAATCTATCTCTGCGAATCTGA5940     AATGGAGTTATTATCTCCCGACATTTAACCTTGGAATGGAAGACCAGTTTAAAATTAATT6000     TAGGCTACAACTACCGCCATATTAATCAAACATCCGAGTTAAACACCCTGGGTGCAACGA6060     AGAAAAAATTTGCAGTATCAGGCGTAAGTGCAGGCATTGATGGACATATCCAATTTACCC6120     CTAAAACAATCTTTAATATTGATTTAACTCATCATTATTACGCGAGTAAATTACCAGGCT6180     CTTTTGGAATGGAGCGCATTGGCGAAACATTTAATCGCAGCTATCACATTAGCACAGCCA6240     GTTTAGGGTTGAGTCAAGAGTTTGCTCAAGGTTGGCATTTTAGCAGTCAATTATCGGGTC6300     AGTTTACTCTACAAGATATAAGTAGCATAGATTTATTCTCTGTAACAGGTACTTATGGCG6360     TCAGAGGCTTTAAATACGGCGGTGCAAGTGGTGAGCGCGGTCTTGTATGGCGTAATGAAT6420     TAAGTATGCCAAAATACACCCGCTTTCAAATCAGCCCTTATGCGTTTTATGATGCAGGTC6480     AGTTCCGTTATAATAGCGAAAATGCTAAAACTTACGGCGAAGATATGCACACGGTATCCT6540     CTGCGGGTTTAGGCATTAAAACCTCTCCTACACAAAACTTAAGCTTAGATGCTTTTGTTG6600     CTCGTCGCTTTGCAAATGCCAATAGTGACAATTTGAATGGCAACAAAAAACGCACAAGCT6660     CACCTACAACCTTCTGGGGTAGATTAACATTCAGTTTCTAACCCTGAAATTTAATCAACT6720     GGTAAGCGTTCCGCCTACCAGTTTATAACTATATGCTTTACCCGCCAATTTACAGTCTAT6780     ACGCAACCCTGTTTTCATCCTTATATATCAAACAAACTAAGCAAACCAAGCAAACCAAGC6840     AAACCAAGCAAACCAAGCAAACCAAGCAAACCAAGCAAACCAAGCAAACCAAGCAAACCA6900     AGCAAACCAAGCAAACCAAGCAAACCAAGCAAACCAAGCAATGCTAAAAAACAATTTATA6960     TGATAAACTAAAACATACTCCATACCATGGCAATACAAGGGATTTAATAATATGACAAAA7020     GAAAATTTACAAAGTGTTCCACAAAATACGACCGCTTCACTTGTAGAATCAAACAACGAC7080     CAAACTTCCCTGCAAATACTTAAACAACCACCCAAACCCAACCTATTACGCCTGGAACAA7140     CATGTCGCCAAAAAAGATTATGAGCTTGCTTGCCGCGAATTAATGGCGATTTTGGAAAAA7200     ATGGACGCTAATTTTGGAGGCGTTCACGATATTGAATTTGACGCACCTGCTCAGCTGGCA7260     TATCTACCCGAAAAACTACTAATTCATTTTGCCACTCGTCTCGCTAATGCAATTACAACA7320     CTCTTTTCCGACCCCGAATTGGCAATTTCCGAAGAAGGGGCATTAAAGATGATTAGCCTG7380     CAACGCTGGTTGACGCTGATTTTTGCCTCTTCCCCCTACGTTAACGCAGACCATATTCTC7440     AATAAATATAATATCAACCCAGATTCCGAAGGTGGCTTTCATTTAGCAACAGACAACTCT7500     TCTATTGCTAAATTCTGTATTTTTTACTTACCCGAATCCAATGTCAATATGAGTTTAGAT7560     GCGTTATGGGCAGGGAATCAACAACTTTGTGCTTCATTGTGTTTTGCGTTGCAGTCTTCA7620     CGTTTTATTGGTACTGCATCTGCGTTTCATAAAAGAGCGGTGGTTTTACAGTGGTTTCCT7680     AAAAAACTCGCCGAAATTGCTAATTTAGATGAATTGCCTGCAAATATCCTTCATGATGTA7740     TATATGCACTGCAGTTATGATTTAGCAAAAAACAAGCACGATGTTAAGCGTCCATTAAAC7800     GAACTTGTCCGCAAGCATATCCTCACGCAAGGATGGCAAGACCGCTACCTTTACACCTTA7860     GGTAAAAAGGACGGCAAACCTGTGATGATGGTACTGCTTGAACATTTTAATTCGGGACAT7920     TCGATTTATCGCACGCATTCAACTTCAATGATTGCTGCTCGAGAAAAATTCTATTTAGTC7980     GGCTTAGGCCATGAGGGCGTTGATAACATAGGTCGAGAAGTGTTTGACGAGTTCTTTGAA8040     ATCAGTAGCAATAATATAATGGAGAGACTGTTTTTTATCCGTAAACAGTGCGAAACTTTC8100     CAACCCGCAGTGTTCTATATGCCAAGCATTGGCATGGATATTACCACGATTTTTGTGAGC8160     AACACTCGGCTTGCCCCTATTCAAGCTGTAGCCTTGGGTCATCCTGCCACTACGCATTCT8220     GAATTTATTGATTATGTCATCGTAGAAGATGATTATGTGGGCAGTGAAGATTGTTTTAGC8280     GAAACCCTTTTACGCTTACCCAAAGATGCCCTACCTTATGTACCATCTGCACTCGCCCCA8340     CAAAAAGTGGATTATGTACTCAGGGAAAACCCTGAAGTAGTCAATATCGGTATTGCCGCT8400     ACCACAATGAAATTAAACCCTGAATTTTTGCTAACATTGCAAGAAATCAGAGATAAAGCT8460     AAAGTCAAAATACATTTTCATTTCGCACTTGGACAATCAACAGGCTTGACACACCCTTAT8520     GTCAAATGGTTTATCGAAAGCTATTTAGGTGACGATGCCACTGCACATCCCCACGCACCT8580     TATCACGATTATCTGGCAATATTGCGTGATTGCGATATGCTACTAAATCCGTTTCCTTTC8640     GGTAATACTAACGGCATAATTGATATGGTTACATTAGGTTTAGTTGGTGTATGCAAAACG8700     GGGGATGAAGTACATGAACATATTGATGAAGGTCTGTTTAAACGCTTAGGACTACCAGAA8760     TGGCTGATAGCCGACACACGAGAAACATATATTGAATGTGCTTTGCGTCTAGCAGAAAAC8820     CATCAAGAACGCCTTGAACTCCGTCGTTACATCATAGAAAACAACGGCTTACAAAAGCTT8880     TTTACAGGCGACCCTCGTCCATTGGGCAAAATACTGCTTAAGAAAACAAATGAATGGAAG8940     CGGAAGCACTTGAGTAAAAAATAACGGTTTTTTAAAGTAAAAGTGCGGTTAATTTTCAAA9000     GCGTTTTAAAAACCTCTCAAAAATCAACCGCACTTTTATCTTTATAACGCTCCCGCGCGC9060     TGACAGTTTATCTCTTTCTTAAAATACCCATAAAATTGTGGCAATAGTTGGGTAATCAAA9120     TTCAATTGTTGATACGGCAAACTAAAGACGGCGCGTTCTTCGGCAGTCATC9171     (2) INFORMATION FOR SEQ ID NO:6:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 9323 base pairs     (B) TYPE: nucleic acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: DNA (genomic)     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:     CGCCACTTCAATTTTGGATTGTTGAAATTCAACTAACCAAAAAGTGCGGTTAAAATCTGT60     GGAGAAAATAGGTTGTAGTGAAGAACGAGGTAATTGTTCAAAAGGATAAAGCTCTCTTAA120     TTGGGCATTGGTTGGCGTTTCTTTTTCGGTTAATAGTAAATTATATTCTGGACGACTATG180     CAATCCACCAACAACTTTACCGTTGGTTTTAAGCGTTAATGTAAGTTCTTGCTCTTCTTG240     GCGAATACGTAATCCCATTTTTTGTTTAGCAAGAAAATGATCGGGATAATCATAATAGGT300     GTTGCCCAAAAATAAATTTTGATGTTCTAAAATCATAAATTTTGCAAGATATTGTGGCAA360     TTCAATACCTATTTGTGGCGAAATCGCCAATTTTAATTCAATTTCTTGTAGCATAATATT420     TCCCACTCAAATCAACTGGTTAAATATACAAGATAATAAAAATAAATCAAGATTTTTGTG480     ATGACAAACAACAATTACAACACCTTTTTTGCAGTCTATATGCAAATATTTTAAAAAAAT540     AGTATAAATCCGCCATATAAAATGGTATAATCTTTCATCTTTCATCTTTCATCTTTCATC600     TTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTCATCTTTC660     ATCTTTCATCTTTCATCTTTCACATGAAATGATGAACCGAGGGAAGGGAGGGAGGGGCAA720     GAATGAAGAGGGAGCTGAACGAACGCAAATGATAAAGTAATTTAATTGTTCAACTAACCT780     TAGGAGAAAATATGAACAAGATATATCGTCTCAAATTCAGCAAACGCCTGAATGCTTTGG840     TTGCTGTGTCTGAATTGGCACGGGGTTGTGACCATTCCACAGAAAAAGGCAGCGAAAAAC900     CTGCTCGCATGAAAGTGCGTCACTTAGCGTTAAAGCCACTTTCCGCTATGTTACTATCTT960     TAGGTGTAACATCTATTCCACAATCTGTTTTAGCAAGCGGCAATTTAACATCGACCAAAA1020     TGAAATGGTGCAGTTTTTACAAGAAAACAAGTAATAAAACCATTATCCGCAACAGTGTTG1080     ACGCTATCATTAATTGGAAACAATTTAACATCGACCAAAATGAAATGGTGCAGTTTTTAC1140     AAGAAAACAACAACTCCGCCGTATTCAACCGTGTTACATCTAACCAAATCTCCCAATTAA1200     AAGGGATTTTAGATTCTAACGGACAAGTCTTTTTAATCAACCCAAATGGTATCACAATAG1260     GTAAAGACGCAATTATTAACACTAATGGCTTTACGGCTTCTACGCTAGACATTTCTAACG1320     AAAACATCAAGGCGCGTAATTTCACCTTCGAGCAAACCAAAGATAAAGCGCTCGCTGAAA1380     TTGTGAATCACGGTTTAATTACTGTCGGTAAAGACGGCAGTGTAAATCTTATTGGTGGCA1440     AAGTGAAAAACGAGGGTGTGATTAGCGTAAATGGTGGCAGCATTTCTTTACTCGCAGGGC1500     AAAAAATCACCATCAGCGATATAATAAACCCAACCATTACTTACAGCATTGCCGCGCCTG1560     AAAATGAAGCGGTCAATCTGGGCGATATTTTTGCCAAAGGCGGTAACATTAATGTCCGTG1620     CTGCCACTATTCGAAACCAAGGTAAACTTTCTGCTGATTCTGTAAGCAAAGATAAAAGCG1680     GCAATATTGTTCTTTCCGCCAAAGAGGGTGAAGCGGAAATTGGCGGTGTAATTTCCGCTC1740     AAAATCAGCAAGCTAAAGGCGGCAAGCTGATGATAAAGTCCGATAAAGTCACATTAAAAA1800     CAGGTGCAGTTATCGACCTTTCAGGTAAAGAAGGGGGAGAAACTTACCTTGGCGGTGACG1860     AGCGCGGCGAAGGTAAAAACGGCATTCAATTAGCAAAGAAAACCTCTTTAGAAAAAGGCT1920     CAACCATCAATGTATCAGGCAAAGAAAAAGGCGGACGCGCTATTGTGTGGGGCGATATTG1980     CGTTAATTGACGGCAATATTAACGCTCAAGGTAGTGGTGATATCGCTAAAACCGGTGGTT2040     TTGTGGAGACATCGGGGCATTATTTATCCATTGACAGCAATGCAATTGTTAAAACAAAAG2100     AGTGGTTGCTAGACCCTGATGATGTAACAATTGAAGCCGAAGACCCCCTTCGCAATAATA2160     CCGGTATAAATGATGAATTCCCAACAGGCACCGGTGAAGCAAGCGACCCTAAAAAAAATA2220     GCGAACTCAAAACAACGCTAACCAATACAACTATTTCAAATTATCTGAAAAACGCCTGGA2280     CAATGAATATAACGGCATCAAGAAAACTTACCGTTAATAGCTCAATCAACATCGGAAGCA2340     ACTCCCACTTAATTCTCCATAGTAAAGGTCAGCGTGGCGGAGGCGTTCAGATTGATGGAG2400     ATATTACTTCTAAAGGCGGAAATTTAACCATTTATTCTGGCGGATGGGTTGATGTTCATA2460     AAAATATTACGCTTGATCAGGGTTTTTTAAATATTACCGCCGCTTCCGTAGCTTTTGAAG2520     GTGGAAATAACAAAGCACGCGACGCGGCAAATGCTAAAATTGTCGCCCAGGGCACTGTAA2580     CCATTACAGGAGAGGGAAAAGATTTCAGGGCTAACAACGTATCTTTAAACGGAACGGGTA2640     AAGGTCTGAATATCATTTCATCAGTGAATAATTTAACCCACAATCTTAGTGGCACAATTA2700     ACATATCTGGGAATATAACAATTAACCAAACTACGAGAAAGAACACCTCGTATTGGCAAA2760     CCAGCCATGATTCGCACTGGAACGTCAGTGCTCTTAATCTAGAGACAGGCGCAAATTTTA2820     CCTTTATTAAATACATTTCAAGCAATAGCAAAGGCTTAACAACACAGTATAGAAGCTCTG2880     CAGGGGTGAATTTTAACGGCGTAAATGGCAACATGTCATTCAATCTCAAAGAAGGAGCGA2940     AAGTTAATTTCAAATTAAAACCAAACGAGAACATGAACACAAGCAAACCTTTACCAATTC3000     GGTTTTTAGCCAATATCACAGCCACTGGTGGGGGCTCTGTTTTTTTTGATATATATGCCA3060     ACCATTCTGGCAGAGGGGCTGAGTTAAAAATGAGTGAAATTAATATCTCTAACGGCGCTA3120     ATTTTACCTTAAATTCCCATGTTCGCGGCGATGACGCTTTTAAAATCAACAAAGACTTAA3180     CCATAAATGCAACCAATTCAAATTTCAGCCTCAGACAGACGAAAGATGATTTTTATGACG3240     GGTACGCACGCAATGCCATCAATTCAACCTACAACATATCCATTCTGGGCGGTAATGTCA3300     CCCTTGGTGGACAAAACTCAAGCAGCAGCATTACGGGGAATATTACTATCGAGAAAGCAG3360     CAAATGTTACGCTAGAAGCCAATAACGCCCCTAATCAGCAAAACATAAGGGATAGAGTTA3420     TAAAACTTGGCAGCTTGCTCGTTAATGGGAGTTTAAGTTTAACTGGCGAAAATGCAGATA3480     TTAAAGGCAATCTCACTATTTCAGAAAGCGCCACTTTTAAAGGAAAGACTAGAGATACCC3540     TAAATATCACCGGCAATTTTACCAATAATGGCACTGCCGAAATTAATATAACACAAGGAG3600     TGGTAAAACTTGGCAATGTTACCAATGATGGTGATTTAAACATTACCACTCACGCTAAAC3660     GCAACCAAAGAAGCATCATCGGCGGAGATATAATCAACAAAAAAGGAAGCTTAAATATTA3720     CAGACAGTAATAATGATGCTGAAATCCAAATTGGCGGCAATATCTCGCAAAAAGAAGGCA3780     ACCTCACGATTTCTTCCGATAAAATTAATATCACCAAACAGATAACAATCAAAAAGGGTA3840     TTGATGGAGAGGACTCTAGTTCAGATGCGACAAGTAATGCCAACCTAACTATTAAAACCA3900     AAGAATTGAAATTGACAGAAGACCTAAGTATTTCAGGTTTCAATAAAGCAGAGATTACAG3960     CCAAAGATGGTAGAGATTTAACTATTGGCAACAGTAATGACGGTAACAGCGGTGCCGAAG4020     CCAAAACAGTAACTTTTAACAATGTTAAAGATTCAAAAATCTCTGCTGACGGTCACAATG4080     TGACACTAAATAGCAAAGTGAAAACATCTAGCAGCAATGGCGGACGTGAAAGCAATAGCG4140     ACAACGATACCGGCTTAACTATTACTGCAAAAAATGTAGAAGTAAACAAAGATATTACTT4200     CTCTCAAAACAGTAAATATCACCGCGTCGGAAAAGGTTACCACCACAGCAGGCTCGACCA4260     TTAACGCAACAAATGGCAAAGCAAGTATTACAACCAAAACAGGTGATATCAGCGGTACGA4320     TTTCCGGTAACACGGTAAGTGTTAGCGCGACTGGTGATTTAACCACTAAATCCGGCTCAA4380     AAATTGAAGCGAAATCGGGTGAGGCTAATGTAACAAGTGCAACAGGTACAATTGGCGGTA4440     CAATTTCCGGTAATACGGTAAATGTTACGGCAAACGCTGGCGATTTAACAGTTGGGAATG4500     GCGCAGAAATTAATGCGACAGAAGGAGCTGCAACCTTAACCGCAACAGGGAATACCTTGA4560     CTACTGAAGCCGGTTCTAGCATCACTTCAACTAAGGGTCAGGTAGACCTCTTGGCTCAGA4620     ATGGTAGCATCGCAGGAAGCATTAATGCTGCTAATGTGACATTAAATACTACAGGCACCT4680     TAACCACCGTGGCAGGCTCGGATATTAAAGCAACCAGCGGCACCTTGGTTATTAACGCAA4740     AAGATGCTAAGCTAAATGGTGATGCATCAGGTGATAGTACAGAAGTGAATGCAGTCAACG4800     ACTGGGGATTTGGTAGTGTGACTGCGGCAACCTCAAGCAGTGTGAATATCACTGGGGATT4860     TAAACACAGTAAATGGGTTAAATATCATTTCGAAAGATGGTAGAAACACTGTGCGCTTAA4920     GAGGCAAGGAAATTGAGGTGAAATATATCCAGCCAGGTGTAGCAAGTGTAGAAGAAGTAA4980     TTGAAGCGAAACGCGTCCTTGAAAAAGTAAAAGATTTATCTGATGAAGAAAGAGAAACAT5040     TAGCTAAACTTGGTGTAAGTGCTGTACGTTTTGTTGAGCCAAATAATACAATTACAGTCA5100     ATACACAAAATGAATTTACAACCAGACCGTCAAGTCAAGTGATAATTTCTGAAGGTAAGG5160     CGTGTTTCTCAAGTGGTAATGGCGCACGAGTATGTACCAATGTTGCTGACGATGGACAGC5220     CGTAGTCAGTAATTGACAAGGTAGATTTCATCCTGCAATGAAGTCATTTTATTTTCGTAT5280     TATTTACTGTGTGGGTTAAAGTTCAGTACGGGCTTTACCCATCTTGTAAAAAATTACGGA5340     GAATACAATAAAGTATTTTTAACAGGTTATTATTATGAAAAATATAAAAAGCAGATTAAA5400     ACTCAGTGCAATATCAGTATTGCTTGGCCTGGCTTCTTCATCATTGTATGCAGAAGAAGC5460     GTTTTTAGTAAAAGGCTTTCAGTTATCTGGTGCACTTGAAACTTTAAGTGAAGACGCCCA5520     ACTGTCTGTAGCAAAATCTTTATCTAAATACCAAGGCTCGCAAACTTTAACAAACCTAAA5580     AACAGCACAGCTTGAATTACAGGCTGTGCTAGATAAGATTGAGCCAAATAAATTTGATGT5640     GATATTGCCGCAACAAACCATTACGGATGGCAATATCATGTTTGAGCTAGTCTCGAAATC5700     AGCCGCAGAAAGCCAAGTTTTTTATAAGGCGAGCCAGGGTTATAGTGAAGAAAATATCGC5760     TCGTAGCCTGCCATCTTTGAAACAAGGAAAAGTGTATGAAGATGGTCGTCAGTGGTTCGA5820     TTTGCGTGAATTTAATATGGCAAAAGAAAACCCGCTTAAGGTTACCCGTGTACATTACGA5880     ACTAAACCCTAAAAACAAAACCTCTAATTTGATAATTGCGGGCTTCTCGCCTTTTGGTAA5940     AACGCGTAGCTTTATTTCTTATGATAATTTCGGCGCGAGAGAGTTTAACTACCAACGTGT6000     AAGCTTGGGTTTTGTTAATGCCAATTTAACTGGTCATGATGATGTGTTAATTATACCAGT6060     ATGAGTTATGCTGATTCTAATGATATCGACGGCTTACCAAGTGCGATTAATCGTAAATTA6120     TCAAAAGGTCAATCTATCTCTGCGAATCTGAAATGGAGTTATTATCTCCCAACATTTAAC6180     CTTGGCATGGAAGACCAATTTAAAATTAATTTAGGCTACAACTACCGCCATATTAATCAA6240     ACCTCCGCGTTAAATCGCTTGGGTGAAACGAAGAAAAAATTTGCAGTATCAGGCGTAAGT6300     GCAGGCATTGATGGACATATCCAATTTACCCCTAAAACAATCTTTAATATTGATTTAACT6360     CATCATTATTACGCGAGTAAATTACCAGGCTCTTTTGGAATGGAGCGCATTGGCGAAACA6420     TTTAATCGCAGCTATCACATTAGCACAGCCAGTTTAGGGTTGAGTCAAGAGTTTGCTCAA6480     GGTTGGCATTTTAGCAGTCAATTATCAGGTCAATTTACTCTACAAGATATTAGCAGTATA6540     GATTTATTCTCTGTAACAGGTACTTATGGCGTCAGAGGCTTTAAATACGGCGGTGCAAGT6600     GGTGAGCGCGGTCTTGTATGGCGTAATGAATTAAGTATGCCAAAATACACCCGCTTCCAA6660     ATCAGCCCTTATGCGTTTTATGATGCAGGTCAGTTCCGTTATAATAGCGAAAATGCTAAA6720     ACTTACGGCGAAGATATGCACACGGTATCCTCTGCGGGTTTAGGCATTAAAACCTCTCCT6780     ACACAAAACTTAAGCCTAGATGCTTTTGTTGCTCGTCGCTTTGCAAATGCCAATAGTGAC6840     AATTTGAATGGCAACAAAAAACGCACAAGCTCACCTACAACCTTCTGGGGGAGATTAACA6900     TTCAGTTTCTAACCCTGAAATTTAATCAACTGGTAAGCGTTCCGCCTACCAGTTTATAAC6960     TATATGCTTTACCCGCCAATTTACAGTCTATAGGCAACCCTGTTTTTACCCTTATATATC7020     AAATAAACAAGCTAAGCTGAGCTAAGCAAACCAAGCAAACTCAAGCAAGCCAAGTAATAC7080     TAAAAAAACAATTTATATGATAAACTAAAGTATACTCCATGCCATGGCGATACAAGGGAT7140     TTAATAATATGACAAAAGAAAATTTGCAAAACGCTCCTCAAGATGCGACCGCTTTACTTG7200     CGGAATTAAGCAACAATCAAACTCCCCTGCGAATATTTAAACAACCACGCAAGCCCAGCC7260     TATTACGCTTGGAACAACATATCGCAAAAAAAGATTATGAGTTTGCTTGTCGTGAATTAA7320     TGGTGATTCTGGAAAAAATGGACGCTAATTTTGGAGGCGTTCACGATATTGAATTTGACG7380     CACCCGCTCAGCTGGCATATCTACCCGAAAAATTACTAATTTATTTTGCCACTCGTCTCG7440     CTAATGCAATTACAACACTCTTTTCCGACCCCGAATTGGCAATTTCTGAAGAAGGGGCGT7500     TAAAGATGATTAGCCTGCAACGCTGGTTGACGCTGATTTTTGCCTCTTCCCCCTACGTTA7560     ACGCAGACCATATTCTCAATAAATATAATATCAACCCAGATTCCGAAGGTGGCTTTCATT7620     TAGCAACAGACAACTCTTCTATTGCTAAATTCTGTATTTTTTACTTACCCGAATCCAATG7680     TCAATATGAGTTTAGATGCGTTATGGGCAGGGAATCAACAACTTTGTGCTTCATTGTGTT7740     TTGCGTTGCAGTCTTCACGTTTTATTGGTACCGCATCTGCGTTTCATAAAAGAGCGGTGG7800     TTTTACAGTGGTTTCCTAAAAAACTCGCCGAAATTGCTAATTTAGATGAATTGCCTGCAA7860     ATATCCTTCATGATGTATATATGCACTGCAGTTATGATTTAGCAAAAAACAAGCACGATG7920     TTAAGCGTCCATTAAACGAACTTGTCCGCAAGCATATCCTCACGCAAGGATGGCAAGACC7980     GCTACCTTTACACCTTAGGTAAAAAGGACGGCAAACCTGTGATGATGGTACTGCTTGAAC8040     ATTTTAATTCGGGACATTCGATTTATCGTACACATTCAACTTCAATGATTGCTGCTCGAG8100     AAAAATTCTATTTAGTCGGCTTAGGCCATGAGGGCGTTGATAAAATAGGTCGAGAAGTGT8160     TTGACGAGTTCTTTGAAATCAGTAGCAATAATATAATGGAGAGACTGTTTTTTATCCGTA8220     AACAGTGCGAAACTTTCCAACCCGCAGTGTTCTATATGCCAAGCATTGGCATGGATATTA8280     CCACGATTTTTGTGAGCAACACTCGGCTTGCCCCTATTCAAGCTGTAGCCCTGGGTCATC8340     CTGCCACTACGCATTCTGAATTTATTGATTATGTCATCGTAGAAGATGATTATGTGGGCA8400     GTGAAGATTGTTTCAGCGAAACCCTTTTACGCTTACCCAAAGATGCCCTACCTTATGTAC8460     CTTCTGCACTCGCCCCACAAAAAGTGGATTATGTACTCAGGGAAAACCCTGAAGTAGTCA8520     ATATCGGTATTGCCGCTACCACAATGAAATTAAACCCTGAATTTTTGCTAACATTGCAAG8580     AAATCAGAGATAAAGCTAAAGTCAAAATACATTTTCATTTCGCACTTGGACAATCAACAG8640     GCTTGACACACCCTTATGTCAAATGGTTTATCGAAAGCTATTTAGGTGACGATGCCACTG8700     CACATCCCCACGCACCTTATCACGATTATCTGGCAATATTGCGTGATTGCGATATGCTAC8760     TAAATCCGTTTCCTTTCGGTAATACTAACGGCATAATTGATATGGTTACATTAGGTTTAG8820     TTGGTGTATGCAAAACGGGGGATGAAGTACATGAACATATTGATGAAGGTCTGTTTAAAC8880     GCTTAGGACTACCAGAATGGCTGATAGCCGACACACGAGAAACATATATTGAATGTGCTT8940     TGCGTCTAGCAGAAAACCATCAAGAACGCCTTGAACTCCGTCGTTACATCATAGAAAACA9000     ACGGCTTACAAAAGCTTTTTACAGGCGACCCTCGTCCATTGGGCAAAATACTGCTTAAGA9060     AAACAAATGAATGGAAGCGGAAGCACTTGAGTAAAAAATAACGGTTTTTTAAAGTAAAAG9120     TGCGGTTAATTTTCAAAGCGTTTTAAAAACCTCTCAAAAATCAACCGCACTTTTATCTTT9180     ATAACGATCCCGCACGCTGACAGTTTATCAGCCTCCCGCCATAAAACTCCGCCTTTCATG9240     GCGGAGATTTTAGCCAAAACTGGCAGAAATTAAAGGCTAAAATCACCAAATTGCACCACA9300     AAATCACCAATACCCACAAAAAA9323     (2) INFORMATION FOR SEQ ID NO:7:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 4287 base pairs     (B) TYPE: nucleic acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: DNA (genomic)     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:     GATCAATCTGGGCGATATTTTTGCCAAAGGTGGTAACATTAATGTCCGCGCTGCCACTAT60     TCGCAATAAAGGTAAACTTTCTGCCGACTCTGTAAGCAAAGATAAAAGTGGTAACATTGT120     TCTCTCTGCCAAAGAAGGTGAAGCGGAAATTGGCGGTGTAATTTCCGCTCAAAATCAGCA180     AGCCAAAGGTGGTAAGTTGATGATTACAGGCGATAAAGTTACATTGAAAACGGGTGCACT240     TATCGACCTTTCGGGTAAAGAAGGGGGAGAAACTTATCTTGGCGGTGACGAGCGTGGCGA300     AGGTAAAAACGGCATTCAATTAGCAAAGAAAACCACTTTAGAAAAAGGCTCAACAATTAA360     TGTGTCAGGTAAAGAAAAAGCTGGGCGCGCTATTGTATGGGGCGATATTGCGTTAATTGA420     CGGCAATATTAATGCCCAAGGTAAAGATATCGCTAAAACTGGTGGTTTTGTGGAGACGTC480     GGGGCATTACTTATCCATTGATGATAACGCAATTGTTAAAACAAAAGAATGGCTACTAGA540     CCCAGAGAATGTGACTATTGAAGCTCCTTCCGCTTCTCGCGTCGAGCTGGGTGCCGATAG600     GAATTCCCACTCGGCAGAGGTGATAAAAGTGACCCTAAAAAAAAATAACACCTCCTTGAC660     AACACTAACCAATACAACCATTTCAAATCTTCTGAAAAGTGCCCACGTGGTGAACATAAC720     GGCAAGGAGAAAACTTACCGTTAATAGCTCTATCAGTATAGAAAGAGGCTCCCACTTAAT780     TCTCCACAGTGAAGGTCAGGGCGGTCAAGGTGTTCAGATTGATAAAGATATTACTTCTGA840     AGGCGGAAATTTAACCATTTATTCTGGCGGATGGGTTGATGTTCATAAAAATATTACGCT900     TGGTAGCGGCTTTTTAAACATCACAACTAAAGAAGGAGATATCGCCTTCGAAGACAAGTC960     TGGACGGAACAACCTAACCATTACAGCCCAAGGGACCATCACCTCAGGTAATAGTAACGG1020     CTTTAGATTTAACAACGTCTCTCTAAACAGCCTTGGCGGAAAGCTGAGCTTTACTGACAG1080     CAGAGAGGACAGAGGTAGAAGAACTAAGGGTAATATCTCAAACAAATTTGACGGAACGTT1140     AAACATTTCCGGAACTGTAGATATCTCAATGAAAGCACCCAAAGTCAGCTGGTTTTACAG1200     AGACAAAGGACGCACCTACTGGAACGTAACCACTTTAAATGTTACCTCGGGTAGTAAATT1260     TAACCTCTCCATTGACAGCACAGGAAGTGGCTCAACAGGTCCAAGCATACGCAATGCAGA1320     ATTAAATGGCATAACATTTAATAAAGCCACTTTTAATATCGCACAAGGCTCAACAGCTAA1380     CTTTAGCATCAAGGCATCAATAATGCCCTTTAAGAGTAACGCTAACTACGCATTATTTAA1440     TGAAGATATTTCAGTCTCAGGGGGGGGTAGCGTTAATTTCAAACTTAACGCCTCATCTAG1500     CAACATACAAACCCCTGGCGTAATTATAAAATCTCAAAACTTTAATGTCTCAGGAGGGTC1560     AACTTTAAATCTCAAGGCTGAAGGTTCAACAGAAACCGCTTTTTCAATAGAAAATGATTT1620     AAACTTAAACGCCACCGGTGGCAATATAACAATCAGACAAGTCGAGGGTACCGATTCACG1680     CGTCAACAAAGGTGTCGCAGCCAAAAAAAACATAACTTTTAAAGGGGGTAATATCACCTT1740     CGGCTCTCAAAAAGCCACAACAGAAATCAAAGGCAATGTTACCATCAATAAAAACACTAA1800     CGCTACTCTTCGTGGTGCGAATTTTGCCGAAAACAAATCGCCTTTAAATATAGCAGGAAA1860     TGTTATTAATAATGGCAACCTTACCACTGCCGGCTCCATTATCAATATAGCCGGAAATCT1920     TACTGTTTCAAAAGGCGCTAACCTTCAAGCTATAACAAATTACACTTTTAATGTAGCCGG1980     CTCATTTGACAACAATGGCGCTTCAAACATTTCCATTGCCAGAGGAGGGGCTAAATTTAA2040     AGATATCAATAACACCAGTAGCTTAAATATTACCACCAACTCTGATACCACTTACCGCAC2100     CATTATAAAAGGCAATATATCCAACAAATCAGGTGATTTGAATATTATTGATAAAAAAAG2160     CGACGCTGAAATCCAAATTGGCGGCAATATCTCACAAAAAGAAGGCAATCTCACAATTTC2220     TTCTGATAAAGTAAATATTACCAATCAGATAACAATCAAAGCAGGCGTTGAAGGGGGGCG2280     TTCTGATTCAAGTGAGGCAGAAAATGCTAACCTAACTATTCAAACCAAAGAGTTAAAATT2340     GGCAGGAGACCTAAATATTTCAGGCTTTAATAAAGCAGAAATTACAGCTAAAAATGGCAG2400     TGATTTAACTATTGGCAATGCTAGCGGTGGTAATGCTGATGCTAAAAAAGTGACTTTTGA2460     CAAGGTTAAAGATTCAAAAATCTCGACTGACGGTCACAATGTAACACTAAATAGCGAAGT2520     GAAAACGTCTAATGGTAGTAGCAATGCTGGTAATGATAACAGCACCGGTTTAACCATTTC2580     CGCAAAAGATGTAACGGTAAACAATAACGTTACCTCCCACAAGACAATAAATATCTCTGC2640     CGCAGCAGGAAATGTAACAACCAAAGAAGGCACAACTATCAATGCAACCACAGGCAGCGT2700     GGAAGTAACTGCTCAAAATGGTACAATTAAAGGCAACATTACCTCGCAAAATGTAACAGT2760     GACAGCAACAGAAAATCTTGTTACCACAGAGAATGCTGTCATTAATGCAACCAGCGGCAC2820     AGTAAACATTAGTACAAAAACAGGGGATATTAAAGGTGGAATTGAATCAACTTCCGGTAA2880     TGTAAATATTACAGCGAGCGGCAATACACTTAAGGTAAGTAATATCACTGGTCAAGATGT2940     AACAGTAACAGCGGATGCAGGAGCCTTGACAACTACAGCAGGCTCAACCATTAGTGCGAC3000     AACAGGCAATGCAAATATTACAACCAAAACAGGTGATATCAACGGTAAAGTTGAATCCAG3060     CTCCGGCTCTGTAACACTTGTTGCAACTGGAGCAACTCTTGCTGTAGGTAATATTTCAGG3120     TAACACTGTTACTATTACTGCGGATAGCGGTAAATTAACCTCCACAGTAGGTTCTACAAT3180     TAATGGGACTAATAGTGTAACCACCTCAAGCCAATCAGGCGATATTGAAGGTACAATTTC3240     TGGTAATACAGTAAATGTTACAGCAAGCACTGGTGATTTAACTATTGGAAATAGTGCAAA3300     AGTTGAAGCGAAAAATGGAGCTGCAACCTTAACTGCTGAATCAGGCAAATTAACCACCCA3360     AACAGGCTCTAGCATTACCTCAAGCAATGGTCAGACAACTCTTACAGCCAAGGATAGCAG3420     TATCGCAGGAAACATTAATGCTGCTAATGTGACGTTAAATACCACAGGCACTTTAACTAC3480     TACAGGGGATTCAAAGATTAACGCAACCAGTGGTACCTTAACAATCAATGCAAAAGATGC3540     CAAATTAGATGGTGCTGCATCAGGTGACCGCACAGTAGTAAATGCAACTAACGCAAGTGG3600     CTCTGGTAACGTGACTGCGAAAACCTCAAGCAGCGTGAATATCACCGGGGATTTAAACAC3660     AATAAATGGGTTAAATATCATTTCGGAAAATGGTAGAAACACTGTGCGCTTAAGAGGCAA3720     GGAAATTGATGTGAAATATATCCAACCAGGTGTAGCAAGCGTAGAAGAGGTAATTGAAGC3780     GAAACGCGTCCTTGAGAAGGTAAAAGATTTATCTGATGAAGAAAGAGAAACACTAGCCAA3840     ACTTGGTGTAAGTGCTGTACGTTTCGTTGAGCCAAATAATGCCATTACGGTTAATACACA3900     AAACGAGTTTACAACCAAACCATCAAGTCAAGTGACAATTTCTGAAGGTAAGGCGTGTTT3960     CTCAAGTGGTAATGGCGCACGAGTATGTACCAATGTTGCTGACGATGGACAGCAGTAGTC4020     AGTAATTGACAAGGTAGATTTCATCCTGCAATGAAGTCATTTTATTTTCGTATTATTTAC4080     TGTGTGGGTTAAAGTTCAGTACGGGCTTTACCCACCTTGTAAAAAATTACGAAAAATACA4140     ATAAAGTATTTTTAACAGGTTATTATTATGAAAAACATAAAAAGCAGATTAAAACTCAGT4200     GCAATATCAATATTGCTTGGCTTGGCTTCTTCATCGACGTATGCAGAAGAAGCGTTTTTA4260     GTAAAAGGCTTTCAGTTATCTGGCGCG4287     (2) INFORMATION FOR SEQ ID NO:8:     (i) SEQUENCE CHARACTERISTICS:     (A) LENGTH: 4702 base pairs     (B) TYPE: nucleic acid     (C) STRANDEDNESS: single     (D) TOPOLOGY: linear     (ii) MOLECULE TYPE: DNA (genomic)     (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:     GGGAATGAGCGTCGTACACGGTACAGCAACCATGCAAGTAGACGGCAATAAAACCACTAT60     CCGTAATAGCATCAATGCTATCATCAATTGGAAACAATTTAACATTGACCAAAATGAAAT120     GGAGCAGTTTTTACAAGAAAGCAGCAACTCTGCCGTTTTCAACCGTGTTACATCTGACCA180     AATCTCCCAATTAAAAGGGATTTTAGATTCTAACGGACAAGTCTTTTTAATCAACCCAAA240     TGGTATCACAATAGGTAAAGACGCAATTATTAACACTAATGGCTTTACTGCTTCTACGCT300     AGACATTTCTAACGAAAACATCAAGGCGCGTAATTTCACCCTTGAGCAAACCAAGGATAA360     AGCACTCGCTGAAATCGTGAATCACGGTTTAATTACCGTTGGTAAAGACGGTAGCGTAAA420     CCTTATTGGTGGCAAAGTGAAAAACGAGGGCGTGATTAGCGTAAATGGCGGTAGTATTTC480     TTTACTTGCAGGGCAAAAAATCACCATCAGCGATATAATAAATCCAACCATCACTTACAG540     CATTGCTGCACCTGAAAACGAAGCGATCAATCTGGGCGATATTTTTGCCAAAGGTGGTAA600     CATTAATGTCCGCGCTGCCACTATTCGCAATAAAGGTAAACTTTCTGCCGACTCTGTAAG660     CAAAGATAAAAGTGGTAACATTGTTCTCTCTGCCAAAGAAGGTGAAGCGGAAATTGGCGG720     TGTAATTTCCGCTCAAAATCAGCAAGCCAAAGGTGGTAAGTTGATGATTACAGGTGATAA780     AGTCACATTAAAAACAGGTGCAGTTATCGACCTTTCAGGTAAAGAAGGGGGAGAGACTTA840     TCTTGGCGGTGATGAGCGTGGCGAAGGTAAAAATGGTATTCAATTAGCGAAGAAAACCTC900     TTTAGAAAAAGGCTCGACAATTAATGTATCAGGCAAAGAAAAAGGCGGGCGCGCTATTGT960     ATGGGGCGATATTGCATTAATTAATGGTAACATTAATGCTCAAGGTAGCGATATTGCTAA1020     AACTGGCGGCTTTGTGGAAACATCAGGACATGACTTATCCATTGGTGATGATGTGATTGT1080     TGACGCTAAAGAGTGGTTATTAGACCCAGATGATGTGTCCATTGAAACTCTTACATCTGG1140     ACGCAATAATACCGGCGAAAACCAAGGATATACAACAGGAGATGGGACTAAAGAGTCACC1200     TAAAGGTAATAGTATTTCTAAACCTACATTAACAAACTCAACTCTTGAGCAAATCCTAAG1260     AAGAGGTTCTTATGTTAATATCACTGCTAATAATAGAATTTATGTTAATAGCTCCATCAA1320     CTTATCTAATGGCAGTTTAACACTTCACACTAAACGAGATGGAGTTAAAATTAACGGTGA1380     TATTACCTCAAACGAAAATGGTAATTTAACCATTAAAGCAGGCTCTTGGGTTGATGTTCA1440     TAAAAACATCACGCTTGGTACGGGTTTTTTCAATATTGTCGCTGGGGATTCTGTAGCTTT1500     TGAGAGAGAGGGCGATAAAGCACGTAACGCAACAGATGCTCAAATTACCGCACAAGGGAC1560     GATAACCGTCAATAAAGATGATAAACAATTTAGATTCAATAATGTATCTATTAACGGGAC1620     GGGCAAGGGTTTAAAGTTTATTGCAAATCAAAATAATTTCACTCATAAATTTGATGGCGA1680     AATTAACATATCTGGAATAGTAACAATTAACCAAACCACGAAAAAAGATGTTAAATACTG1740     GAATGCATCAAAAGACTCTTACTGGAATGTTTCTTCTCTTACTTTGAATACGGTGCAAAA1800     ATTTACCTTTATAAAATTCGTTGATAGCGGCTCAAATTCCCAAGATTTGAGGTCATCACG1860     TAGAAGTTTTGCAGGCGTACATTTTAACGGCATCGGAGGCAAAACAAACTTCAACATCGG1920     AGCTAACGCAAAAGCCTTATTTAAATTAAAACCAAACGCCGCTACAGACCCAAAAAAAGA1980     ATTACCTATTACTTTTAACGCCAACATTACAGCTACCGGTAACAGTGATAGCTCTGTGAT2040     GTTTGACATACACGCCAATCTTACCTCTAGAGCTGCCGGCATAAACATGGATTCAATTAA2100     CATTACCGGCGGGCTTGACTTTTCCATAACATCCCATAATCGCAATAGTAATGCTTTTGA2160     AATCAAAAAAGACTTAACTATAAATGCAACTGGCTCGAATTTTAGTCTTAAGCAAACGAA2220     AGATTCTTTTTATAATGAATACAGCAAACACGCCATTAACTCAAGTCATAATCTAACCAT2280     TCTTGGCGGCAATGTCACTCTAGGTGGGGAAAATTCAAGCAGTAGCATTACGGGCAATAT2340     CAATATCACCAATAAAGCAAATGTTACATTACAAGCTGACACCAGCAACAGCAACACAGG2400     CTTGAAGAAAAGAACTCTAACTCTTGGCAATATATCTGTTGAGGGGAATTTAAGCCTAAC2460     TGGTGCAAATGCAAACATTGTCGGCAATCTTTCTATTGCAGAAGATTCCACATTTAAAGG2520     AGAAGCCAGTGACAACCTAAACATCACCGGCACCTTTACCAACAACGGTACCGCCAACAT2580     TAATATAAAACAAGGAGTGGTAAAACTCCAAGGCGATATTATCAATAAAGGTGGTTTAAA2640     TATCACTACTAACGCCTCAGGCACTCAAAAAACCATTATTAACGGAAATATAACTAACGA2700     AAAAGGCGACTTAAACATCAAGAATATTAAAGCCGACGCCGAAATCCAAATTGGCGGCAA2760     TATCTCACAAAAAGAAGGCAATCTCACAATTTCTTCTGATAAAGTAAATATTACCAATCA2820     GATAACAATCAAAGCAGGCGTTGAAGGGGGGCGTTCTGATTCAAGTGAGGCAGAAAATGC2880     TAACCTAACTATTCAAACCAAAGAGTTAAAATTGGCAGGAGACCTAAATATTTCAGGCTT2940     TAATAAAGCAGAAATTACAGCTAAAAATGGCAGTGATTTAACTATTGGCAATGCTAGCGG3000     TGGTAATGCTGATGCTAAAAAAGTGACTTTTGACAAGGTTAAAGATTCAAAAATCTCGAC3060     TGACGGTCACAATGTAACACTAAATAGCGAAGTGAAAACGTCTAATGGTAGTAGCAATGC3120     TGGTAATGATAACAGCACCGGTTTAACCATTTCCGCAAAAGATGTAACGGTAAACAATAA3180     CGTTACCTCCCACAAGACAATAAATATCTCTGCCGCAGCAGGAAATGTAACAACCAAAGA3240     AGGCACAACTATCAATGCAACCACAGGCAGCGTGGAAGTAACTGCTCAAAATGGTACAAT3300     TAAAGGCAACATTACCTCGCAAAATGTAACAGTGACAGCAACAGAAAATCTTGTTACCAC3360     AGAGAATGCTGTCATTAATGCAACCAGCGGCACAGTAAACATTAGTACAAAAACAGGGGA3420     TATTAAAGGTGGAATTGAATCAACTTCCGGTAATGTAAATATTACAGCGAGCGGCAATAC3480     ACTTAAGGTAAGTAATATCACTGGTCAAGATGTAACAGTAACAGCGGATGCAGGAGCCTT3540     GACAACTACAGCAGGCTCAACCATTAGTGCGACAACAGGCAATGCAAATATTACAACCAA3600     AACAGGTGATATCAACGGTAAAGTTGAATCCAGCTCCGGCTCTGTAACACTTGTTGCAAC3660     TGGAGCAACTCTTGCTGTAGGTAATATTTCAGGTAACACTGTTACTATTACTGCGGATAG3720     CGGTAAATTAACCTCCACAGTAGGTTCTACAATTAATGGGACTAATAGTGTAACCACCTC3780     AAGCCAATCAGGCGATATTGAAGGTACAATTTCTGGTAATACAGTAAATGTTACAGCAAG3840     CACTGGTGATTTAACTATTGGAAATAGTGCAAAAGTTGAAGCGAAAAATGGAGCTGCAAC3900     CTTAACTGCTGAATCAGGCAAATTAACCACCCAAACAGGCTCTAGCATTACCTCAAGCAA3960     TGGTCAGACAACTCTTACAGCCAAGGATAGCAGTATCGCAGGAAACATTAATGCTGCTAA4020     TGTGACGTTAAATACCACAGGCACTTTAACTACTACAGGGGATTCAAAGATTAACGCAAC4080     CAGTGGTACCTTAACAATCAATGCAAAAGATGCCAAATTAGATGGTGCTGCATCAGGTGA4140     CCGCACAGTAGTAAATGCAACTAACGCAAGTGGCTCTGGTAACGTGACTGCGAAAACCTC4200     AAGCAGCGTGAATATCACCGGGGATTTAAACACAATAAATGGGTTAAATATCATTTCGGA4260     AAATGGTAGAAACACTGTGCGCTTAAGAGGCAAGGAAATTGATGTGAAATATATCCAACC4320     AGGTGTAGCAAGCGTAGAAGAGGTAATTGAAGCGAAACGCGTCCTTGAGAAGGTAAAAGA4380     TTTATCTGATGAAGAAAGAGAAACACTAGCCAAACTTGGTGTAAGTGCTGTACGTTTCGT4440     TGAGCCAAATAATGCCATTACGGTTAATACACAAAACGAGTTTACAACCAAACCATCAAG4500     TCAAGTGACAATTTCTGAAGGTAAGGCGTGTTTCTCAAGTGGTAATGGCGCACGAGTATG4560     TACCAATGTTGCTGACGATGGACAGCAGTAGTCAGTAATTGACAAGGTAGATTTCATCCT4620     GCAATGAAGTCATTTTATTTTCGTATTATTTACTGTGTGGGTTAAAGTTCAGTACGGGCT4680     TTACCCACCTTGTAAAAAATTA4702     __________________________________________________________________________ 

What we claim is:
 1. A vaccine against diseased caused by non-typeable Haemophilus influenza, including otitis media, sinusitis and bronchitis, which comprises a mixture of (1) HMW1 encoded by the DNA sequence shown in FIG. 1 (SEQ ID No:1), having the derived amino acid sequence of FIG. 2 (SEQ ID No:2) and having an apparent molecular weight of 125 kDa and (2) HMW2 encoded by the DNA sequence shown in FIG. 3 (SEQ ID No:3), having the derived amino acid sequence of FIG. 4 (SEQ ID No:4) and having an apparent molecular weight of 120 kDa, and a physiological carrier for said mixture. 